coronary products catalog

W i n t e r 2 0 1 2

Coronary ProductsCatalog

At Medtronic, we’re committed to innovating for life by pushing the boundaries of medical technology and changing the way the world treats chronic disease. Our innovations help physicians diagnose diseases earlier, treat patients with minimal disruptions and alleviate pain and symptoms throughout patients’ lives. To do that, we think beyond the status quo—relentlessly seeking improved ways to help people live better, longer and more productive lives.

The Medtronic CardioVascular business, our third largest, spans the major specialties of interventional cardiology and cardiac and vascular surgery. Our products, developed in collaboration with leading physicians, are used to reduce the potentially debilitating effects of coronary, aortic and structural heart disease.*

Through continued innovation and collaboration, we are pleased to offer one of the most comprehensive coronary product portfolios for the treatment of coronary artery disease.

Sincerely,

Jason FontanaVice President, U.S. Coronary Therapy Strategy and Development

* This catalog only covers percutaneous coronary interventional products. Please contact LifeLine CardioVascular Technical Support for information on other cardiovascular products.

Coronary Products Catalog W I N T E R 2 0 1 2

Drug-Eluting Stents

resolute integrity Zotarolimus-eluting Coronary Stent: rX Coronary Stent System . . . . . . . . . . . . . . . . . . . . . . . . . 1 OtW Coronary Stent System . . . . . . . . . . . . . . . . . . . . . . . 3endeavor® Sprint Zotarolimus-eluting Coronary Stent: rX Coronary Stent System . . . . . . . . . . . . . . . . . . . . . . . . . 5 OtW Coronary Stent System . . . . . . . . . . . . . . . . . . . . . . . 6

Bare Metal Stents

integrity® Bare Metal CoronaryStent: rX Coronary Stent System . . . . . . . . . . . . . . . . . . . . . . . . . 7 OtW Coronary Stent System . . . . . . . . . . . . . . . . . . . . . . . 9

Balloon Dilatation Catheters

Sprinter® Legend Semicompliant. . . . . . . . . . . . . . . . . . . . . . . 11Sprinter® Legend 1.25 mm . . . . . . . . . . . . . . . . . . . . . . . . . . . 12Sprinter® OtW Semicompliant . . . . . . . . . . . . . . . . . . . . . . . . 13nC Sprinter® rX noncompliant . . . . . . . . . . . . . . . . . . . . . . . . 14nC Stormer® OtW noncompliant . . . . . . . . . . . . . . . . . . . . . . 15

Guide Catheters

Launcher® Guide Catheters . . . . . . . . . . . . . . . . . . . . . . . . . . 17 LeftCoronary/17•RightCoronary/19•Radial/21•Other/22Sherpa nX Guide Catheters nX Active. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25 LeftCoronary/25•RightCoronary/27•Radial/29•Other/30 nX Balanced. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32 LeftCoronary/32•RightCoronary/34•Radial/36•Other/37Z2® Guide Catheters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39 LeftCoronary/39•RightCoronary/41•Other/43Zuma® Guide Catheters . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45 LeftCoronary/45•RightCoronary/47•Other/49

Embolic Protection

export® AP Aspiration Catheter . . . . . . . . . . . . . . . . . . . . . . . 51export® Xt Aspiration Catheter . . . . . . . . . . . . . . . . . . . . . . . . 52GuardWire® temporary Occlusion and Aspiration System . . . . . . . 52

Interventional Guidewires (0.014 in.)

Zinger® Stainless Steel Workhorse . . . . . . . . . . . . . . . . . . . . . . 53intuition Stainless Steel Advanced Workhorse . . . . . . . . . . . . . . 55Cougar® nitinol Workhorse . . . . . . . . . . . . . . . . . . . . . . . . . . 56thunder® Stainless Steel extra-Support . . . . . . . . . . . . . . . . . . 57ProVia Stainless Steel Crossing . . . . . . . . . . . . . . . . . . . . . . . 58

(continued on next page)

Contents, continued

Diagnostics and Accessories

Angiographic Catheters . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59 SiteSeer® . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59 Pro-Flo® . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 70 Sones® Woven Coronary Catheters . . . . . . . . . . . . . . . . . . . 80 Woven Coronary Catheters—High-Volume . . . . . . . . . . . . . 83 Woven Coronary Catheters—General Purpose and transvalvular Catheters . . . . . . . . . . . . . . . . . . . . . . . . . 84Introducers input® tS introducer Sheaths . . . . . . . . . . . . . . . . . . . . . . . 85 input® PS introducer Sheaths . . . . . . . . . . . . . . . . . . . . . . . 86 input® Accessories (obturators, vessel dilators, sterile sleeves) . . 87 input® SSV Split-Away Sheath with Valve and Side Port . . . . . . 88 transseptal Catheter introducer Sheaths . . . . . . . . . . . . . . . 89Interventional Accessories everest inflation Device and Survival Kit . . . . . . . . . . . . . . . . 91 Piton® Disposable Adapters . . . . . . . . . . . . . . . . . . . . . . . . 92 Stretch insertion tool, Steering Handles . . . . . . . . . . . . . . . . 92Pediatric Products Pediatric Woven Coronary Catheters . . . . . . . . . . . . . . . . . . 93 Pediatric Woven niH Catheters . . . . . . . . . . . . . . . . . . . . . . 94 Pediatric rashkind® Septostomy Balloon Catheters . . . . . . . . . 95 Brockenbrough® needles. . . . . . . . . . . . . . . . . . . . . . . . . . 96 Pediatric Mullins transseptal introducer Sheath . . . . . . . . . . . 96Hemodynamic Monitoring Catheter Pulmonary Wedge Pressure (PWP) Catheter . . . . . . . . . . . . . 97Angiographic Guidewires Stainless Steel Guidewires . . . . . . . . . . . . . . . . . . . . . . . . . 99 PtFe-Coated Guidewires: Fixed Core . . . . . . . . . . . . . . . . . . 100 PtFe-Coated Guidewires: Movable Core . . . . . . . . . . . . . . . . 101 Heparin over PtFe-Coated Guidewires . . . . . . . . . . . . . . . . . 101 Specialty Guidewires . . . . . . . . . . . . . . . . . . . . . . . . . . . . 102Transseptal Products Brockenbrough® needles . . . . . . . . . . . . . . . . . . . . . . . . . 105 transseptal Catheter introducer Sheaths. . . . . . . . . . . . . . . . 105

Contact and Ordering Information

Contact and Ordering information . . . . . . . . . . . . . . . . . . . . . 107 Reimbursement•TechSupport•Ordering•Shipping•Returns . . . 1072011 Coronary Diagnostic and intervention Coding Sheet . . . . . . 109

ii

1

Drug-Eluting Coronary Stents

Resolute Integrity RX Ordering Information

Resolute Integrity RX Compliance

0.91 mm (2.7 F)distal shaft

Proximal and distalradiopaque markers

0.69 mm (2.1 F)proximal shaft

Minimal balloonoverhang

Nominal pressure Rated burst pressure*

*Rated burst pressure—do not exceed.

† Do not postdilate the 2.25–2.75-mm stents to greater than 3.50 mm. Do not postdilate the 3.00–4.00-mm stents to greater than 4.75 mm.

Crossing profiles:

2.25–2.75 mm: 0.97–1.04 mm (0.038–0.040 in.)3.0–4.0 mm: 1.04–1.19 mm (0.041–0.047 in.)

Stent Diameter (mm)

Stent Length (mm)

8 9 12 14 15 18 22 26 30

2.25 RSINT22508UX — RSINT22512UX RSINT22514UX — RSINT22518UX RSINT22522UX RSINT22526UX RSINT22530UX



3.00 — RSINT30009UX RSINT30012UX — RSINT30015UX RSINT30018UX RSINT30022UX RSINT30026UX RSINT30030UX



For distribution in the USA only. © 2012 Medtronic, inc. All rights reserved. UC201204308en 2/12

Resolute Integrity Drug-Eluting RX Coronary Stent System General Characteristics:

Supplied sterile.items per box: 1

Resolute Integrity DES, built on the Integrity® platform, delivers a powerful antiproliferative, zotarolimus, via the BioLinx® biocompatible polymer. The low-profile, cobalt-alloy stent is mounted on the extended pressure, semicompliant, RX MicroTrac delivery system.

Pressure(atm)

Stent Diameter Deployed Stent i.D. (mm)

2.25† 2.50† 2.75† 3.00† 3.50† 4.00†

6 2.20 2.45 2.70 2.90 3.30 3.757 2.20 2.45 2.70 2.95 3.35 3.808 2.25 2.50 2.75 3.00 3.40 3.909 2.30 2.55 2.80 3.05 3.50 3.95

10 2.30 2.60 2.85 3.10 3.55 4.0511 2.35 2.60 2.90 3.15 3.60 4.1012 2.40 2.65 2.95 3.20 3.65 4.1513 2.40 2.70 3.00 3.20 3.70 4.2014 2.45 2.70 3.05 3.25 3.75 4.2515 2.50 2.75 3.10 3.30 3.80 4.3016 2.55 2.80 3.15 3.35 3.85 4.3517 2.60 2.80 3.20 3.40 3.90 4.4018 2.60 2.85 3.25 3.45 3.95 4.4519 — 2.90 3.30 3.50 4.00 4.5020 — 2.95 3.40 3.55 4.05 —

2

C O R O N A R YDrug-Eluting Stents

IndicationsThe Resolute Integrity Zotarolimus-Eluting Coronary Stent System is indicated for improving coronary luminal diameters in patients, including those with diabetes mellitus, with symptomatic ischemic heart disease due to de novo lesions of length ≤ 27 mm in native coronary arteries with reference vessel diameters of 2.25 mm to 4.20 mm.ContraindicationsTheResoluteIntegrityZotarolimus-ElutingCoronaryStentSystemiscontraindicatedforusein:•Patientswith a known hypersensitivity or allergies to aspirin, heparin, bivalirudin, clopidogrel, prasugrel, ticagrelor, ticlopidine, drugs such as zotarolimus, tacrolimus, sirolimus, everolimus or similar drugs or any other analogueorderivative•Patientswithaknownhypersensitivitytothecobalt-basedalloy(cobalt,nickel,chromiumandmolybdenum)•PatientswithaknownhypersensitivitytotheBioLinx® polymer or its individual components Coronaryarterystentingiscontraindicatedforusein:•Patientsinwhomantiplateletand/oranticoagulationtherapyiscontraindicated•Patientswhoarejudgedtohavealesionthatpreventscomplete inflation of an angioplasty balloon or proper placement of the stent or stent delivery systemwarnings•Pleaseensurethattheinnerpackagehasnotbeenopenedordamagedasthiswouldindicatethesterilebarrierhasbeenbreached.•Theuseofthisproductcarriesthesamerisksassociatedwithcoronaryarterystent implantation procedures, which include subacute and late vessel thrombosis, vascular complications and/orbleedingevents.•Thisproductshouldnotbeusedinpatientswhoarenotlikelytocomplywiththerecommended antiplatelet therapy.Precautions•Onlyphysicianswhohavereceivedadequatetrainingshouldperformimplantationofthestent.•Stentplacement should only be performed at hospitals where emergency coronary artery bypass graft surgery canbereadilyperformed.•Subsequentstentrestenosisorocclusionmayrequirerepeatcatheter-basedtreatments (including balloon dilatation) of the arterial segment containing the stent. The long-term outcome following repeat catheter-based treatments of previously implanted endothelialized stents is notwellcharacterized.•Therisksandbenefitsofthestentimplantationshouldbeassessedforpatientswithahistoryofseverereactiontocontrastagents.•Donotexposeorwipetheproductwithorganicsolventssuchasalcohol.•Whendrug-elutingstents(DES)areusedoutsidethespecifiedIndications for Use, patientoutcomesmaydifferfromtheresultsobservedintheRESOLUTEpivotalclinicaltrials.•Comparedto use within the specified Indications for Use, the use of DES in patients and lesions outside of the labeled indications, including more tortuous anatomy, may have an increased risk of adverse events, including stentthrombosis,stentembolization,myocardialinfarction(MI),ordeath•Careshouldbetakentocontrolthe position of the guide catheter tip during stent delivery, deployment, and balloon withdrawal. Before withdrawing the stent delivery system, visually confirm complete balloon deflation by fluoroscopy to avoid guidingcathetermovementintothevesselandsubsequentarterialdamage•Stentthrombosisisalow-frequency event that is frequently associated with MI or death. Data from the RESOLUTE clinical trials have been prospectively evaluated and adjudicated using the definition developed by the Academic Research Consortium (ARC).

The safety and effectiveness of the Resolute Integrity stent have not yet been established in the following patientpopulations:•Patientswithtargetlesionswhichweretreatedwithpriorbrachytherapyortheuseofbrachytherapytotreatin-stentrestenosisofaResoluteIntegritystent•Womenwhoarepregnantorlactating•Menintendingtofatherchildren•Pediatricpatients•Patientswithcoronaryarteryreferencevesseldiametersof<2.25mmor>4.20mm•Patientswithcoronaryarterylesionslongerthan27mmorrequiringmorethanoneResoluteIntegritystent•PatientswithevidenceofanacuteMIwithin72hoursofintendedstentimplantation•Patientswithvesselthrombusatthelesionsite•Patientswithlesionslocatedinasaphenousveingraft,intheleftmaincoronaryartery,ostiallesions,orbifurcationlesions•Patientswithdiffusediseaseorpoorflowdistaltoidentifiedlesions•Patientswithtortuousvesselsintheregionofthetargetvesselorproximaltothelesion•Patientswithin-stentrestenosis•Patientswithmoderateorseverelesioncalcificationatthetargetlesion•Patientswithoccludedtargetlesionsincludingchronictotalocclusions•Patientswiththree-vesseldisease•Patientswithaleftventricularejectionfractionof<30% •Patientswithaserumcreatinineof>2.5mg/dl•Patientswithlongerthan24monthsoffollow-upThe safety and effectiveness of the Resolute Integrity stent have not been established in the cerebral, carotid or peripheral vasculature.Potential Adverse EventsOther risks associated with using this device are those associated with percutaneous coronary diagnostic (including angiography and IVUS) and treatment procedures. These risks (in alphabetical order) may includebutarenotlimitedto:•Abruptvesselclosure•Accesssitepain,hematomaorhemorrhage•Allergicreaction(tocontrast,antiplatelettherapy,stentmaterial,ordrugandpolymercoating)•Aneurysm,pseudoaneurysm,orarteriovenousfistula(AVF)•Arrhythmias,includingventricularfibrillation•Balloonrupture•Bleeding•Cardiactamponade•Coronaryarteryocclusion,perforation,ruptureordissection •Coronaryarteryspasm•Death•Embolism(air,tissue,deviceorthrombus)•Emergencysurgery:peripheralvascularorcoronarybypass•Failuretodeliverthestent•Hemorrhagerequiringtransfusion•Hypotension/hypertension•Incompletestentapposition•Infectionorfever•MI•Pericarditis•Peripheralischemia/peripheralnerveinjury•Renalfailure•Restenosisofthestentedartery•Shock/pulmonaryedema•Stableorunstableangina•Stentdeformation,collapse,orfracture•Stentmigration(orembolization)•Stentmisplacement•Stroke/transientischemicattack•Thrombosis(acute,subacuteorlate)Adverse Events Related to Zotarolimus Patients’ exposure to zotarolimus is directly related to the total amount of stent length implanted. The actual side effects/complications that may be associated with the use of zotarolimus are not fully known. The adverse events that have been associated with the intravenous injection of zotarolimus in humans includebutarenotlimitedto:•Anemia•Diarrhea•Dryskin•Headache•Hematuria•Infection•Injectionsitereaction•Pain(abdominal,arthralgia,injectionsite)•RashPlease reference appropriate product Instructions for Use for more information regarding indications, warnings, precautions and potential adverse events.CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.


3


Resolute Integrity DES, built on the Integrity® platform, delivers a powerful antiproliferative, zotarolimus, via the BioLinx® biocompatible polymer. The low-profile, cobalt-alloy stent is mounted on the extended pressure, semicompliant, OTW MicroTrac delivery system.


Stent Diameter (mm)

Stent Length (mm)8 9 12 14 15 18 22 26 30

2.25 RSINT22508W — RSINT22512W RSINT22514W — RSINT22518W RSINT22522W RSINT22526W RSINT22530W



3.00 — RSINT30009W RSINT30012W — RSINT30015W RSINT30018W RSINT30022W RSINT30026W RSINT30030W



Resolute Integrity OTw Ordering Information

Resolute Integrity Drug-Eluting OTw Coronary Stent System

Resolute Integrity OTw Compliance





Pressure(atm)


2.25† 2.50† 2.75† 3.00† 3.50† 4.00†

6 2.20 2.45 2.70 2.90 3.30 3.757 2.20 2.45 2.70 2.95 3.35 3.808 2.25 2.50 2.75 3.00 3.40 3.909 2.30 2.55 2.80 3.05 3.50 3.95

10 2.30 2.60 2.85 3.10 3.55 4.0511 2.35 2.60 2.90 3.15 3.60 4.1012 2.40 2.65 2.95 3.20 3.65 4.1513 2.40 2.70 3.00 3.20 3.70 4.2014 2.45 2.70 3.05 3.25 3.75 4.2515 2.50 2.75 3.10 3.30 3.80 4.3016 2.55 2.80 3.15 3.35 3.85 4.3517 2.60 2.80 3.20 3.40 3.90 4.4018 2.60 2.85 3.25 3.45 3.95 4.4519 — 2.90 3.30 3.50 4.00 4.5020 — 2.95 3.40 3.55 4.05 —



Crossing profiles:

2.25–2.75 mm: 0.97–1.04 mm (0.038–0.040 in.) 3.0–4.0 mm: 1.04–1.19 mm (0.041–0.047 in.)

General Characteristics:Supplied sterile.items per box: 1


4


IndicationsThe Resolute Integrity Zotarolimus-Eluting Coronary Stent System is indicated for improving coronary luminal diameters in patients, including those with diabetes mellitus, with symptomatic ischemic heart disease due to de novo lesions of length ≤ 27 mm in native coronary arteries with reference vessel diameters of 2.25 mm to 4.20 mm.ContraindicationsTheResoluteIntegrityZotarolimus-ElutingCoronaryStentSystemiscontraindicatedforusein:•Patientswith a known hypersensitivity or allergies to aspirin, heparin, bivalirudin, clopidogrel, prasugrel, ticagrelor, ticlopidine, drugs such as zotarolimus, tacrolimus, sirolimus, everolimus or similar drugs or any other analogueorderivative•Patientswithaknownhypersensitivitytothecobalt-basedalloy(cobalt,nickel,chromiumandmolybdenum)•PatientswithaknownhypersensitivitytotheBioLinx® polymer or its individual components Coronaryarterystentingiscontraindicatedforusein:•Patientsinwhomantiplateletand/oranticoagulationtherapyiscontraindicated•Patientswhoarejudgedtohavealesionthatpreventscomplete inflation of an angioplasty balloon or proper placement of the stent or stent delivery systemwarnings•Pleaseensurethattheinnerpackagehasnotbeenopenedordamagedasthiswouldindicatethesterilebarrierhasbeenbreached.•Theuseofthisproductcarriesthesamerisksassociatedwithcoronaryarterystent implantation procedures, which include subacute and late vessel thrombosis, vascular complications and/orbleedingevents.•Thisproductshouldnotbeusedinpatientswhoarenotlikelytocomplywiththerecommended antiplatelet therapy.Precautions•Onlyphysicianswhohavereceivedadequatetrainingshouldperformimplantationofthestent.•Stentplacement should only be performed at hospitals where emergency coronary artery bypass graft surgery canbereadilyperformed.•Subsequentstentrestenosisorocclusionmayrequirerepeatcatheter-basedtreatments (including balloon dilatation) of the arterial segment containing the stent. The long-term outcome following repeat catheter-based treatments of previously implanted endothelialized stents is notwellcharacterized.•Therisksandbenefitsofthestentimplantationshouldbeassessedforpatientswithahistoryofseverereactiontocontrastagents.•Donotexposeorwipetheproductwithorganicsolventssuchasalcohol.•Whendrug-elutingstents(DES)areusedoutsidethespecifiedIndications for Use, patientoutcomesmaydifferfromtheresultsobservedintheRESOLUTEpivotalclinicaltrials.•Comparedto use within the specified Indications for Use, the use of DES in patients and lesions outside of the labeled indications, including more tortuous anatomy, may have an increased risk of adverse events, including stentthrombosis,stentembolization,myocardialinfarction(MI),ordeath•Careshouldbetakentocontrolthe position of the guide catheter tip during stent delivery, deployment, and balloon withdrawal. Before withdrawing the stent delivery system, visually confirm complete balloon deflation by fluoroscopy to avoid guidingcathetermovementintothevesselandsubsequentarterialdamage•Stentthrombosisisalow-frequency event that is frequently associated with MI or death. Data from the RESOLUTE clinical trials have been prospectively evaluated and adjudicated using the definition developed by the Academic Research Consortium (ARC).

The safety and effectiveness of the Resolute Integrity stent have not yet been established in the following patientpopulations:•Patientswithtargetlesionswhichweretreatedwithpriorbrachytherapyortheuseofbrachytherapytotreatin-stentrestenosisofaResoluteIntegritystent•Womenwhoarepregnantorlactating•Menintendingtofatherchildren•Pediatricpatients•Patientswithcoronaryarteryreferencevesseldiametersof<2.25mmor>4.20mm•Patientswithcoronaryarterylesionslongerthan27mmorrequiringmorethanoneResoluteIntegritystent•PatientswithevidenceofanacuteMIwithin72hoursofintendedstentimplantation•Patientswithvesselthrombusatthelesionsite•Patientswithlesionslocatedinasaphenousveingraft,intheleftmaincoronaryartery,ostiallesions,orbifurcationlesions•Patientswithdiffusediseaseorpoorflowdistaltoidentifiedlesions•Patientswithtortuousvesselsintheregionofthetargetvesselorproximaltothelesion•Patientswithin-stentrestenosis•Patientswithmoderateorseverelesioncalcificationatthetargetlesion•Patientswithoccludedtargetlesionsincludingchronictotalocclusions•Patientswiththree-vesseldisease•Patientswithaleftventricularejectionfractionof<30% •Patientswithaserumcreatinineof>2.5mg/dl•Patientswithlongerthan24monthsoffollow-upThe safety and effectiveness of the Resolute Integrity stent have not been established in the cerebral, carotid or peripheral vasculature.Potential Adverse EventsOther risks associated with using this device are those associated with percutaneous coronary diagnostic (including angiography and IVUS) and treatment procedures. These risks (in alphabetical order) may includebutarenotlimitedto:•Abruptvesselclosure•Accesssitepain,hematomaorhemorrhage•Allergicreaction(tocontrast,antiplatelettherapy,stentmaterial,ordrugandpolymercoating)•Aneurysm,pseudoaneurysm,orarteriovenousfistula(AVF)•Arrhythmias,includingventricularfibrillation•Balloonrupture•Bleeding•Cardiactamponade•Coronaryarteryocclusion,perforation,ruptureordissection •Coronaryarteryspasm•Death•Embolism(air,tissue,deviceorthrombus)•Emergencysurgery:peripheralvascularorcoronarybypass•Failuretodeliverthestent•Hemorrhagerequiringtransfusion•Hypotension/hypertension•Incompletestentapposition•Infectionorfever•MI•Pericarditis•Peripheralischemia/peripheralnerveinjury•Renalfailure•Restenosisofthestentedartery•Shock/pulmonaryedema•Stableorunstableangina•Stentdeformation,collapse,orfracture•Stentmigration(orembolization)•Stentmisplacement•Stroke/transientischemicattack•Thrombosis(acute,subacuteorlate)Adverse Events Related to Zotarolimus Patients’ exposure to zotarolimus is directly related to the total amount of stent length implanted. The actual side effects/complications that may be associated with the use of zotarolimus are not fully known. The adverse events that have been associated with the intravenous injection of zotarolimus in humans includebutarenotlimitedto:•Anemia•Diarrhea•Dryskin•Headache•Hematuria•Infection•Injectionsitereaction•Pain(abdominal,arthralgia,injectionsite)•RashPlease reference appropriate product Instructions for Use for more information regarding indications, warnings, precautions and potential adverse events.CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.


5


© 2009 Medtronic, inc. All rights reserved. UC200904590en 3/09

3.3 F proximal shaft Minimal balloon overhang

2.7 F distal shaft Proximal and distal radiopaque

markers

3.0 F intermediate shaft

Endeavor® Sprint Zotarolimus-Eluting RX Coronary Stent System

Endeavor Sprint RX Ordering Information

Balloon Diameter (mm)

Length (mm) Crossing Profile O.D. mm (in.)8 9 12 14 15 18 24 30

2.50 ENSP25008UX — ENSP25012UX ENSP25014UX — ENSP25018UX ENSP25024UX ENSP25030UX 1.02–1.04 (0.040–0.041)

3.00 — ENSP30009UX ENSP30012UX — ENSP30015UX ENSP30018UX ENSP30024UX ENSP30030UX 1.09–1.12 (0.043–0.044)

3.50 — ENSP35009UX ENSP35012UX — ENSP35015UX ENSP35018UX ENSP35024UX ENSP35030UX 1.09–1.12 (0.043–0.044)

Endeavor Sprint RX ComplianceTechnical Information5 F minimum guide catheter i.D.: 1.4 mm (0.056 in.)


The Endeavor zotarolimus-eluting coronary stent system is a low-profile, modular, cobalt alloy drug-eluting stent that effectively combines the deliverability of the Driver® stent platform with a highly lipophilic sirolimus analog and a clinically established PC polymer. The Endeavor stent is mounted on an extended-pressure, semicompliant rapid exchange delivery system and features minimal balloon overhang.

CAUTION: Do not dilate the stent beyond these limits.

Nominal Stent Diameter

DilatationLimits

2.5 mm 3.0 mm3.0 mm 3.5 mm3.5 mm 4.0 mm

Pressure (atm)

Deployed Stent I.D. (mm)2.50 3.00 3.50

6 2.43 2.88 3.317 2.48 2.93 3.368 2.53 2.99 3.439 2.58 3.05 3.49

10 2.62 3.11 3.5611 2.65 3.15 3.6012 2.69 3.18 3.6413 2.72 3.22 3.6814 2.75 3.25 3.7115 2.79 3.29 3.7516 2.83 3.33 3.7817 2.86 3.37 3.82

Rated burst pressure*

Nominal pressure

Nominal pressure: the pressure at which the balloon reaches its labeled diameter. Rated burst pressure: the maximum pressure to which a balloon is designed to be inflated (95% confidence that 99.9% will not fail below rated burst pressure).

* Rated burst pressure—do not exceed. Test data on file at Medtronic, Inc.

IndicationsThe Endeavor® Sprint Zotarolimus-Eluting Coronary Stent Delivery System is indicated for improving coronary luminal diameter in patients with ischemic heart disease due to de novo lesions of length ≤27 mm in native coronary arteries with reference vessel diameters of ≥2.5 mm to ≤3.5 mm.ContraindicationsThe Endeavor Zotarolimus-Eluting Coronary Stent System is contraindicated for use in:•Patientswithaknownhypersensitivitytozotarolimusorstructurally-relatedcompounds•Patientswithaknownhypersensitivitytothecobalt-basedalloy(cobalt,nickel,chromium,andmolybdenum)•Patientswith a known hypersensitivity to Phosphorylcholine polymer or its individual components.Coronary artery stenting is contraindicated for use in:•Patientswithaknownhypersensitivityorallergiestoaspirin,heparin,clopidogrelorticlopidine•Patientswhocannotreceiverecommendedantiplateletand/oranticoagulationtherapy•Patientswhoarejudgedto have a lesion that prevents complete inflation of an angioplasty balloon or proper placement of the stent or stent delivery system.warnings•Pleaseensurethattheinnerpackagehasnotbeenopenedordamaged,asthisindicatesthesterilebarrierhasbeenbreached•Theuseofthisproductcarriestherisksassociatedwithcoronaryarterystenting,includingsubacutethrombosis,vascularcomplications,and/orbleedingevents•Thisproductshouldnotbe used in patients who are not likely to comply with the recommended antiplatelet therapy.Precautions•Onlyphysicianswhohavereceivedadequatetrainingshouldperformimplantationofthestent•Stentplacement should only be performed at hospitals where emergency coronary artery bypass graft surgery canbereadilyperformed•Subsequentstentblockagemayrequirerepeatdilatationofthearterialsegmentcontaining the stent. The long-term outcome following repeat dilatation of endothelialized stents is not wellcharacterized•Risksandbenefitsofthestentshouldbeassessedforpatientswithhistoryofseverereactiontocontrastagents•Donotexposeorwipetheproductwithorganicsolventssuchasalcoholordetergents•Stentthrombosisisalow-frequencyeventthatcurrentdrug-elutingstent(DES)clinicaltrialsare not adequately powered to fully characterize. Stent thrombosis is frequently associated with myocardial infarction (MI) or death. Data from the ENDEAVOR randomized clinical trials have been prospectively evaluated and adjudicated using both the protocol definition of stent thrombosis and the definition developed by the Academic Research Consortium (ARC), and demonstrate specific patterns of stent thrombosis that vary depending on the definition used. In the ENDEAVOR clinical trials analyzed to date, the differences in the incidence of stent thrombosis observed with the Endeavor stent compared to bare metal stents have not been associated with an increased risk of cardiac death, MI, or all-cause mortality. Additional data from longer-term follow-up in the ENDEAVOR randomized clinical trials and analyses of DES-related stent thrombosis are expected and should be considered in making treatment decisions as data become available•WhenDESareusedoutsidethespecifiedIndications for Use, patient outcomes may differ from the resultsobservedinthepivotalclinicaltrials•ComparedtousewithinthespecifiedIndications for Use, the use of DES in patients and lesions outside of the labeled indications, including more tortuous anatomy, may have

an increased risk of adverse events, including stent thrombosis, stent embolization, MI, or death.The safety and effectiveness of the Endeavor stent have not yet been established in the following patient populations:•Womenwhoarepregnantorlactating•Menintendingtofatherchildren•Pediatricpatients•Patientswithvesselthrombusatthelesionsite•Patientswithcoronaryarteryreferencevesseldiameters<2.5mmor>3.5mm•Patientswithcoronaryarterylesionslongerthan27mmorrequiringmorethanoneEndeavorstent•Patientswithlesionslocatedinsaphenousveingrafts,intheunprotectedleftmaincoronaryartery,ostiallesions,orlesionslocatedatabifurcation•Patientswithdiffusediseaseorpoorflowdistaltotheidentifiedlesions•Patientswithmultivesseldisease•Patientswithtortuousvesselsintheregionoftheobstructionorproximaltothelesion•Patientswitharecentacutemyocardialinfarctionwherethereisevidenceofthrombusorpoorflow•Patientsforlongerthan48monthsoffollow-up•Patientswithin-stentrestenosis•Patientswithmoderateorseverecalcificationinthelesionorachronictotalocclusion•Patientswith prior brachytherapy of the target lesion or the use of brachytherapy to treat in-stent restenosis in an Endeavor stent. The safety and effectiveness of the Endeavor stent have not been established in the cerebral, carotid, or peripheral vasculature.Potential Adverse EventsOther risks associated with using this device are those associated with percutaneous coronary diagnostic (including angiography and IVUS) and treatment procedures. These risks may include, but are not limited to•Abruptvesselclosure•Accesssitepain,hematomaorhemorrhage•Allergicreaction(tocontrast,antiplatelettherapy,stentmaterial,ordrugandpolymercoating)•Aneurysm,pseudoaneurysm,orarteriovenous fistula (AVF) •Arrhythmias•Balloonrupture•Cardiactamponade•Coronaryarteryocclusion,perforation,rupture,ordissection•Coronaryarteryspasm•Death•Embolism(air,tissue,device,orthrombus) •Emergencysurgery:peripheralvascularorcoronarybypass•Failuretodeliverthestent•Hemorrhagerequiringtransfusion•Hypotension/hypertension•Incompletestentapposition•Infectionorfever•Lateorverylatethrombosis•Myocardialinfarction(MI)•Myocardialischemia•Peripheralischemia/peripheralnerveinjury•Renalfailure•Restenosisofthestentedartery•Ruptureofnativeorbypassgraft•Shock/pulmonaryedema•Stentdeformation,collapse,orfracture•Stentmigration•Stentmisplacement•Stroke/transientischemicattack•Thrombosis(acuteandsubacute)•Unstableangina•Ventricularfibrillation.Adverse Events Related to Zotarolimus Patients’ exposure to zotarolimus is directly related to the total amount of stent length implanted. The actual side effects/complications that may be associated with the use of zotarolimus are not fully known. The adverse events that have been associated with the intravenous injection of zotarolimus in humans include•Anemia•Applicationsitereaction•Diarrhea•Dryskin•Headache•Hematuria•Infection•Injectionsitereaction•Pain(abdominal,arthralgia,injectionsite)•Rash.Please reference appropriate product Instructions for Use for more information regarding indications, warnings, precautions and potential adverse events.CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.

6


* Rated burst pressure—do not exceed. Test data on file at Medtronic, Inc.

Endeavor® Sprint Zotarolimus-Eluting OTw Coronary Stent System

Endeavor Sprint OTw Ordering Information


Length (mm) Crossing Profile O.D. mm (in.)8 9 12 14 15 18 24 30

2.50 ENSP25008W — ENSP25012W ENSP25014W — ENSP25018W ENSP25024W ENSP25030W 1.02–1.04 (0.040–0.041)

3.00 — ENSP30009W ENSP30012W — ENSP30015W ENSP30018W ENSP30024W ENSP30030W 1.09–1.12 (0.043–0.044)

3.50 — ENSP35009W ENSP35012W — ENSP35015W ENSP35018W ENSP35024W ENSP35030W 1.09–1.12 (0.043–0.044)

Endeavor Sprint OTw ComplianceTechnical Information5 F minimum guide catheter i.D.: 1.4 mm (0.056 in.)


The Endeavor zotarolimus-eluting coronary stent system is a low-profile, modular, cobalt alloy drug-eluting stent that effectively combines the deliverability of the Driver® stent platform with a highly lipophilic sirolimus analog and a clinically established PC polymer. The Endeavor stent is mounted on an extended-pressure, semicompliant over-the-wire delivery system and features minimal balloon overhang.

3.3 F proximal shaft

Minimal balloon overhang

2.7 F distal shaft Proximal and distal radiopaque

markers

3.0 F intermediate shaft

Pressure (atm)

Deployed Stent I.D. (mm)2.50 3.00 3.50

6 2.43 2.88 3.317 2.48 2.93 3.368 2.53 2.99 3.439 2.58 3.05 3.49

10 2.62 3.11 3.5611 2.65 3.15 3.6012 2.69 3.18 3.6413 2.72 3.22 3.6814 2.75 3.25 3.7115 2.79 3.29 3.7516 2.83 3.33 3.7817 2.86 3.37 3.82

CAUTION: Do not dilate the stent beyond these limits.

Nominal Stent Diameter

DilatationLimits

2.5 mm 3.0 mm3.0 mm 3.5 mm3.5 mm 4.0 mm


Nominal pressure


IndicationsThe Endeavor® Sprint Zotarolimus-Eluting Coronary Stent Delivery System is indicated for improving coronary luminal diameter in patients with ischemic heart disease due to de novo lesions of length ≤27 mm in native coronary arteries with reference vessel diameters of ≥2.5 mm to ≤3.5 mm.ContraindicationsThe Endeavor Zotarolimus-Eluting Coronary Stent System is contraindicated for use in:•Patientswithaknownhypersensitivitytozotarolimusorstructurally-relatedcompounds•Patientswithaknownhypersensitivitytothecobalt-basedalloy(cobalt,nickel,chromium,andmolybdenum)•Patientswith a known hypersensitivity to Phosphorylcholine polymer or its individual components.Coronary artery stenting is contraindicated for use in:•Patientswithaknownhypersensitivityorallergiestoaspirin,heparin,clopidogrelorticlopidine•Patientswhocannotreceiverecommendedantiplateletand/oranticoagulationtherapy•Patientswhoarejudgedto have a lesion that prevents complete inflation of an angioplasty balloon or proper placement of the stent or stent delivery system.warnings•Pleaseensurethattheinnerpackagehasnotbeenopenedordamaged,asthisindicatesthesterilebarrierhasbeenbreached•Theuseofthisproductcarriestherisksassociatedwithcoronaryarterystenting,includingsubacutethrombosis,vascularcomplications,and/orbleedingevents•Thisproductshouldnotbe used in patients who are not likely to comply with the recommended antiplatelet therapy.Precautions•Onlyphysicianswhohavereceivedadequatetrainingshouldperformimplantationofthestent•Stentplacement should only be performed at hospitals where emergency coronary artery bypass graft surgery canbereadilyperformed•Subsequentstentblockagemayrequirerepeatdilatationofthearterialsegmentcontaining the stent. The long-term outcome following repeat dilatation of endothelialized stents is not wellcharacterized•Risksandbenefitsofthestentshouldbeassessedforpatientswithhistoryofseverereactiontocontrastagents•Donotexposeorwipetheproductwithorganicsolventssuchasalcoholordetergents•Stentthrombosisisalow-frequencyeventthatcurrentdrug-elutingstent(DES)clinicaltrialsare not adequately powered to fully characterize. Stent thrombosis is frequently associated with myocardial infarction (MI) or death. Data from the ENDEAVOR randomized clinical trials have been prospectively evaluated and adjudicated using both the protocol definition of stent thrombosis and the definition developed by the Academic Research Consortium (ARC), and demonstrate specific patterns of stent thrombosis that vary depending on the definition used. In the ENDEAVOR clinical trials analyzed to date, the differences in the incidence of stent thrombosis observed with the Endeavor stent compared to bare metal stents have not been associated with an increased risk of cardiac death, MI, or all-cause mortality. Additional data from longer-term follow-up in the ENDEAVOR randomized clinical trials and analyses of DES-related stent thrombosis are expected and should be considered in making treatment decisions as data become available•WhenDESareusedoutsidethespecifiedIndications for Use, patient outcomes may differ from the resultsobservedinthepivotalclinicaltrials•ComparedtousewithinthespecifiedIndications for Use, the use of DES in patients and lesions outside of the labeled indications, including more tortuous anatomy, may have

an increased risk of adverse events, including stent thrombosis, stent embolization, MI, or death.The safety and effectiveness of the Endeavor stent have not yet been established in the following patient populations:•Womenwhoarepregnantorlactating•Menintendingtofatherchildren•Pediatricpatients•Patientswithvesselthrombusatthelesionsite•Patientswithcoronaryarteryreferencevesseldiameters<2.5mmor>3.5mm•Patientswithcoronaryarterylesionslongerthan27mmorrequiringmorethanoneEndeavorstent•Patientswithlesionslocatedinsaphenousveingrafts,intheunprotectedleftmaincoronaryartery,ostiallesions,orlesionslocatedatabifurcation•Patientswithdiffusediseaseorpoorflowdistaltotheidentifiedlesions•Patientswithmultivesseldisease•Patientswithtortuousvesselsintheregionoftheobstructionorproximaltothelesion•Patientswitharecentacutemyocardialinfarctionwherethereisevidenceofthrombusorpoorflow•Patientsforlongerthan48monthsoffollow-up•Patientswithin-stentrestenosis•Patientswithmoderateorseverecalcificationinthelesionorachronictotalocclusion•Patientswith prior brachytherapy of the target lesion or the use of brachytherapy to treat in-stent restenosis in an Endeavor stent. The safety and effectiveness of the Endeavor stent have not been established in the cerebral, carotid, or peripheral vasculature.Potential Adverse EventsOther risks associated with using this device are those associated with percutaneous coronary diagnostic (including angiography and IVUS) and treatment procedures. These risks may include, but are not limited to•Abruptvesselclosure•Accesssitepain,hematomaorhemorrhage•Allergicreaction(tocontrast,antiplatelettherapy,stentmaterial,ordrugandpolymercoating)•Aneurysm,pseudoaneurysm,orarteriovenous fistula (AVF) •Arrhythmias•Balloonrupture•Cardiactamponade•Coronaryarteryocclusion,perforation,rupture,ordissection•Coronaryarteryspasm•Death•Embolism(air,tissue,device,orthrombus) •Emergencysurgery:peripheralvascularorcoronarybypass•Failuretodeliverthestent•Hemorrhagerequiringtransfusion•Hypotension/hypertension•Incompletestentapposition•Infectionorfever•Lateorverylatethrombosis•Myocardialinfarction(MI)•Myocardialischemia•Peripheralischemia/peripheralnerveinjury•Renalfailure•Restenosisofthestentedartery•Ruptureofnativeorbypassgraft•Shock/pulmonaryedema•Stentdeformation,collapse,orfracture•Stentmigration•Stentmisplacement•Stroke/transientischemicattack•Thrombosis(acuteandsubacute)•Unstableangina•Ventricularfibrillation.Adverse Events Related to Zotarolimus Patients’ exposure to zotarolimus is directly related to the total amount of stent length implanted. The actual side effects/complications that may be associated with the use of zotarolimus are not fully known. The adverse events that have been associated with the intravenous injection of zotarolimus in humans include•Anemia•Applicationsitereaction•Diarrhea•Dryskin•Headache•Hematuria•Infection•Injectionsitereaction•Pain(abdominal,arthralgia,injectionsite)•Rash.Please reference appropriate product Instructions for Use for more information regarding indications, warnings, precautions and potential adverse events.CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.

© 2009 Medtronic, inc. All rights reserved. UC200904589en 3/09

7

Integrity RX Ordering Information

Integrity® RX Coronary Stent System

Integrity RX Compliance


The Integrity bare metal coronary stent system incorporates continuous sinusoid technology in an advanced, low-profile cobalt alloy stent that is mounted on the extended-pressure, semicompliant RX MicroTrac delivery system.





Pressure(atm)


2.25† 2.50† 2.75† 3.00† 3.50† 4.00†

6 2.15 2.40 2.65 2.85 3.25 3.707 2.20 2.45 2.70 2.90 3.30 3.758 2.20 2.50 2.75 2.95 3.40 3.859 2.25 2.55 2.80 3.05 3.45 3.90

10 2.30 2.55 2.85 3.10 3.50 4.0011 2.35 2.60 2.90 3.10 3.55 4.0512 2.35 2.65 2.90 3.15 3.60 4.1013 2.40 2.65 2.95 3.20 3.65 4.1514 2.45 2.70 3.00 3.25 3.65 4.2015 2.50 2.75 3.05 3.30 3.70 4.2516 2.50 2.80 3.10 3.30 3.75 4.3017 2.55 2.80 3.15 3.35 3.80 4.3518 2.60 2.85 3.20 3.40 3.85 4.4019 2.65 2.90 3.25 3.45 3.90 4.4520 2.75 2.95 3.30 3.50 3.90 —




Crossing profiles:

2.25–2.75 mm: 0.97–1.04 mm (0.038–0.040 in.)3.0–4.0 mm: 1.04–1.19 mm (0.041–0.047 in.)

Stent Diameter (mm)

Stent Length (mm)8 9 12 14 15 18 22 26 30

2.25 INT22508UX — INT22512UX INT22514UX — INT22518UX INT22522UX INT22526UX —2.50 INT25008UX — INT25012UX INT25014UX — INT25018UX INT25022UX INT25026UX —2.75 INT27508UX — INT27512UX INT27514UX — INT27518UX INT27522UX INT27526UX —3.00 — INT30009UX INT30012UX — INT30015UX INT30018UX INT30022UX INT30026UX INT30030UX3.50 — INT35009UX INT35012UX — INT35015UX INT35018UX INT35022UX INT35026UX INT35030UX4.00 — INT40009UX INT40012UX — INT40015UX INT40018UX INT40022UX INT40026UX INT40030UX

For distribution in the USA only. © 2011 Medtronic, inc. All rights reserved. UC201101771aen 10/11

Bare Metal Coronary Stents

8

C O R O N A R YBare Metal Stents

Indications for UseThe Integrity Coronary Stent Systems are indicated for improving coronary luminal diameter in patients with symptomatic ischemic heart disease due to discrete de novo or restenotic lesions with reference vessel diameters of 2.25–4.0 mm and ≤30 mm in length using direct stenting or predilatation.Contraindications •Patientsinwhomantiplateletand/or

anticoagulation therapy is contraindicated •Patientswhoarejudgedtohavealesionthat

prevents complete inflation of an angioplasty balloon or proper placement of a stent or stent delivery system

warnings/PrecautionsThe long-term effects of stents and the risks associated with lifelong carrying of these implants are unknown. This lack of knowledge should be considered in making a risk/benefit assessment for the patient prior to implantation. •TheIntegrityCoronaryStentSystemsare

provided sterile, for one procedure only. Do not resterilize. Use by the “Use by” date noted on the package.•Onlyphysicianswhohavereceived

appropriate training should perform implantation of the stent. Use of an Integrity Coronary Stent System requires advanced coronary angioplasty technical skills. The instructions will give technical guidance, but do not obviate the need for formal training in the use of the device.•Patientsallergictocobaltalloymaysufferan

allergic reaction to this implant. •Donotremovethestentfromthestent

delivery system; the stent cannot be removed and placed on another balloon catheter for deployment.•Donottrytostraightenakinkedshaftor

hypotube. Straightening a kinked metal shaft may result in breakage of the shaft. If the device is kinked, it should not be used.•Significantamountsofairintheballoonmay

cause uneven expansion of the stent and difficulty in deployment of the stent. Do not pre-inflate balloon prior to stent deployment. Use balloon preparation technique described within this instructional material.

•TheIntegrityCoronaryStentSystemsdonotprovide for distal dye injections or pressure measurements through the guidewire lumen.•Expansionofthestentshouldnotbe

undertaken if the stent is not appropriately positioned in the vessel. If the position of the stent is not optimal, it should not be expanded. •Incompletedeploymentofthestent(i.e.,stent

not fully expanded) may cause procedural complications resulting in patient injury. •AdvancementofanIntegrityCoronaryStent

System through a previously stented segment may cause procedural complications resulting in patient injury.•Placementofthestenthasthepotentialto

compromise sidebranch patency.•Administerappropriateanticoagulant/

antiplatelet and coronary artery vasodilator therapy according to current medical guidelines and manufacturer’s instructions.•Cautionmustbetakenwhenusingancillary

equipment, such as intravascular ultrasound catheters, to avoid dislodgement or deformation of the stent.•Whenmultiplestentsarerequired,stent

materials should be of similar composition. Placing multiple stents of different materials in contact with each other may increase the potential for corrosion. Data obtained from in vitro corrosion tests using a cobalt alloy stent (Medtronic Integrity Coronary Stent) in combination with a stainless steel alloy stent (Boston Scientific Liberté® Coronary Stent) do not suggest an increased risk of in vivo corrosion. •Whenusingtwowires,careshouldbetaken

when introducing, torquing and removing one or both guidewires to avoid entanglement. It is recommended that one guidewire be completely withdrawn from the patient before removing any additional equipment. •Stentplacementshouldonlybeperformed

at hospitals where emergency coronary artery bypass graft surgery can be readily performed.•Judiciousselectionofpatientsisnecessary

since the use of this device carries the associated risk of subacute thrombosis,

vascular complications and/or bleeding events. Administration of appropriate anticoagulant, antiplatelet and coronary vasodilator therapy is critical to successful stent implantation and follow-up. •Subsequentrestenosismayrequirerepeat

dilatation of the arterial segment containing the stent. The long-term outcome following repeat dilatation of endothelialized coronary stents is unknown at present.

Potential Adverse EventsThe following complications may be associated with the use of coronary stenting devices or PTCA:•Acutemyocardialinfarction•Allergicreactionto contrast medium/stent material/medications •Arrhythmias(includingventricularfibrillationandventriculartachycardia)•Arteriovenousfistula • Bleeding complications • Cardiactamponade•Cerebrovascularaccident/stroke•Death•Dissectionofcoronaryartery•Drugreactions•Embolization(air,stent,tissueorthrombotic)•Emergencycoronaryarterybypassgraftsurgery(CABG)•Endocarditis•Failuretodeliverthestent•Stentdeformation,collapseorfracture•Hematoma•Hemorrhagerequiringtransfusion•Injuryofthecoronaryartery•Myocardialischemia/infarction•Painandtendernessattheinsertionsite•Perforation•PeripheralIschemia•Peripheralnerveinjury•Pseudoaneurysm(coronary/femoral/radial)•Pyrogenicreaction•Restenosisofthedilatedarteryorstentedsegment•Sepsis/infection•Short-termhemodynamicdeterioration(hypotension/hypertension)•Stentthrombosisorocclusion•Totalocclusionofcoronaryartery•Unstableangina•Vascularthrombosis•Vesseldissection/perforation/spasm

Please reference appropriate product Instructions for Use for a more detailed list of indications, warnings, precautions and potential adverse events.

CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.


9


Stent Diameter (mm)

Stent Length (mm)8 9 12 14 15 18 22 26 30

2.25 INT22508W — INT22512W INT22514W — INT22518W INT22522W INT22526W —2.50 INT25008W — INT25012W INT25014W — INT25018W INT25022W INT25026W —2.75 INT27508W — INT27512W INT27514W — INT27518W INT27522W INT27526W —3.00 — INT30009W INT30012W — INT30015W INT30018W INT30022W INT30026W INT30030W3.50 — INT35009W INT35012W — INT35015W INT35018W INT35022W INT35026W INT35030W4.00 — INT40009W INT40012W — INT40015W INT40018W INT40022W INT40026W INT40030W

Integrity OTw Ordering Information

Integrity® OTw Coronary Stent System

Integrity OTw Compliance





Pressure(atm)


2.25† 2.50† 2.75† 3.00† 3.50† 4.00†

6 2.15 2.40 2.65 2.85 3.25 3.707 2.20 2.45 2.70 2.90 3.30 3.758 2.20 2.50 2.75 2.95 3.40 3.859 2.25 2.55 2.80 3.05 3.45 3.90

10 2.30 2.55 2.85 3.10 3.50 4.0011 2.35 2.60 2.90 3.10 3.55 4.0512 2.35 2.65 2.90 3.15 3.60 4.1013 2.40 2.65 2.95 3.20 3.65 4.1514 2.45 2.70 3.00 3.25 3.65 4.2015 2.50 2.75 3.05 3.30 3.70 4.2516 2.50 2.80 3.10 3.30 3.75 4.3017 2.55 2.80 3.15 3.35 3.80 4.3518 2.60 2.85 3.20 3.40 3.85 4.4019 2.65 2.90 3.25 3.45 3.90 4.4520 2.75 2.95 3.30 3.50 3.90 —



Crossing profiles:

2.25–2.75 mm: 0.97–1.04 mm (0.038–0.040 in.) 3.0–4.0 mm: 1.04–1.19 mm (0.041–0.047 in.)


The Integrity bare metal coronary stent system incorporates continuous sinusoid technology in an advanced, low-profile cobalt alloy stent that is mounted on the extended-pressure, semi-compliant OTW MicroTrac delivery system.



10


Indications for UseThe Integrity Coronary Stent Systems are indicated for improving coronary luminal diameter in patients with symptomatic ischemic heart disease due to discrete de novo or restenotic lesions with reference vessel diameters of 2.25–4.0 mm and ≤30 mm in length using direct stenting or predilatation.Contraindications •Patientsinwhomantiplateletand/or

anticoagulation therapy is contraindicated •Patientswhoarejudgedtohavealesionthat

prevents complete inflation of an angioplasty balloon or proper placement of a stent or stent delivery system

warnings/PrecautionsThe long-term effects of stents and the risks associated with lifelong carrying of these implants are unknown. This lack of knowledge should be considered in making a risk/benefit assessment for the patient prior to implantation. •TheIntegrityCoronaryStentSystemsare

provided sterile, for one procedure only. Do not resterilize. Use by the “Use by” date noted on the package.•Onlyphysicianswhohavereceived

appropriate training should perform implantation of the stent. Use of an Integrity Coronary Stent System requires advanced coronary angioplasty technical skills. The instructions will give technical guidance, but do not obviate the need for formal training in the use of the device.•Patientsallergictocobaltalloymaysufferan

allergic reaction to this implant. •Donotremovethestentfromthestent

delivery system; the stent cannot be removed and placed on another balloon catheter for deployment.•Donottrytostraightenakinkedshaftor

hypotube. Straightening a kinked metal shaft may result in breakage of the shaft. If the device is kinked, it should not be used.•Significantamountsofairintheballoonmay

cause uneven expansion of the stent and difficulty in deployment of the stent. Do not pre-inflate balloon prior to stent deployment. Use balloon preparation technique described within this instructional material.

•TheIntegrityCoronaryStentSystemsdonotprovide for distal dye injections or pressure measurements through the guidewire lumen.•Expansionofthestentshouldnotbe

undertaken if the stent is not appropriately positioned in the vessel. If the position of the stent is not optimal, it should not be expanded. •Incompletedeploymentofthestent(i.e.,stent

not fully expanded) may cause procedural complications resulting in patient injury. •AdvancementofanIntegrityCoronaryStent

System through a previously stented segment may cause procedural complications resulting in patient injury.•Placementofthestenthasthepotentialto

compromise sidebranch patency.•Administerappropriateanticoagulant/

antiplatelet and coronary artery vasodilator therapy according to current medical guidelines and manufacturer’s instructions.•Cautionmustbetakenwhenusingancillary

equipment, such as intravascular ultrasound catheters, to avoid dislodgement or deformation of the stent.•Whenmultiplestentsarerequired,stent

materials should be of similar composition. Placing multiple stents of different materials in contact with each other may increase the potential for corrosion. Data obtained from in vitro corrosion tests using a cobalt alloy stent (Medtronic Integrity Coronary Stent) in combination with a stainless steel alloy stent (Boston Scientific Liberté® Coronary Stent) do not suggest an increased risk of in vivo corrosion. •Whenusingtwowires,careshouldbetaken

when introducing, torquing and removing one or both guidewires to avoid entanglement. It is recommended that one guidewire be completely withdrawn from the patient before removing any additional equipment. •Stentplacementshouldonlybeperformed

at hospitals where emergency coronary artery bypass graft surgery can be readily performed.•Judiciousselectionofpatientsisnecessary

since the use of this device carries the associated risk of subacute thrombosis,

vascular complications and/or bleeding events. Administration of appropriate anticoagulant, antiplatelet and coronary vasodilator therapy is critical to successful stent implantation and follow-up. •Subsequentrestenosismayrequirerepeat

dilatation of the arterial segment containing the stent. The long-term outcome following repeat dilatation of endothelialized coronary stents is unknown at present.

Potential Adverse EventsThe following complications may be associated with the use of coronary stenting devices or PTCA:•Acutemyocardialinfarction•Allergicreactionto contrast medium/stent material/medications •Arrhythmias(includingventricularfibrillationandventriculartachycardia)•Arteriovenousfistula • Bleeding complications • Cardiactamponade•Cerebrovascularaccident/stroke•Death•Dissectionofcoronaryartery•Drugreactions•Embolization(air,stent,tissueorthrombotic)•Emergencycoronaryarterybypassgraftsurgery(CABG)•Endocarditis•Failuretodeliverthestent•Stentdeformation,collapseorfracture•Hematoma•Hemorrhagerequiringtransfusion•Injuryofthecoronaryartery•Myocardialischemia/infarction•Painandtendernessattheinsertionsite•Perforation•PeripheralIschemia•Peripheralnerveinjury•Pseudoaneurysm(coronary/femoral/radial)•Pyrogenicreaction•Restenosisofthedilatedarteryorstentedsegment•Sepsis/infection•Short-termhemodynamicdeterioration(hypotension/hypertension)•Stentthrombosisorocclusion•Totalocclusionofcoronaryartery•Unstableangina•Vascularthrombosis•Vesseldissection/perforation/spasm

Please reference appropriate product Instructions for Use for a more detailed list of indications, warnings, precautions and potential adverse events.

CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.


11

Pressure(atm)

Balloon Diameter (mm)RX/OTw RX

1.25 1.50 2.00 2.25 2.50 2.75 3.00 3.25 3.50 3.75 4.004 0.60 1.36 — — — — — — — — —5 0.60 1.41 — — — — — — — — —6 0.63 1.47 1.91 2.23 2.34 2.60 2.81 3.14 3.32 3.61 3.857 0.67 1.53 1.95 2.29 2.41 2.67 2.89 3.22 3.42 3.70 3.968 0.75 1.58 2.00 2.33 2.47 2.74 2.97 3.29 3.50 3.79 4.059 0.86 1.61 2.03 2.38 2.53 2.79 3.04 3.35 3.57 3.86 4.12

10 0.99 1.64 2.06 2.41 2.57 2.84 3.09 3.40 3.63 3.93 4.1811 1.11 1.67 2.09 2.44 2.61 2.89 3.14 3.44 3.68 3.98 4.2312 1.20 1.70 2.12 2.47 2.64 2.93 3.18 3.48 3.73 4.02 4.2913 1.28 1.73 2.14 2.51 2.67 2.96 3.22 3.52 3.77 4.07 4.3514 1.35 1.75 2.16 2.54 2.70 3.00 3.25 3.56 3.82 4.12 4.4015 1.40 1.78 2.19 2.58 2.73 3.03 3.29 3.59 3.87 4.16 4.4516 — — 2.21 2.61 2.76 3.07 3.33 3.64 3.92 4.21 4.50

Sprinter® Legend Semicompliant Balloon Dilatation Catheter


Compatible with 6 F kissing balloon technique.

Any combination of two Sprinter Legend rapid exchange balloon models (1.25– 3.50 mm) can be used for the kissing balloon technique within a 6 F (MGCID 0.070”) guide catheter. Test data on file at Medtronic, Inc.


Balloon Length (mm) Crossing Profile O.D. mm (in.)6 10 12 15 20 25 30

1.25 SPL12506X SPL12510X SPL12512X SPL12515X SPL12520X — — 0.5 (0.020)1.50 SPL15006X SPL15010X SPL15012X SPL15015X SPL15020X — — 0.5 (0.021)2.00 SPL20006X SPL20010X SPL20012X SPL20015X SPL20020X SPL20025X SPL20030X 0.6 (0.022)2.25 SPL22506X SPL22510X SPL22512X SPL22515X SPL22520X SPL22525X — 0.6 (0.022)2.50 SPL25006X SPL25010X SPL25012X SPL25015X SPL25020X SPL25025X SPL25030X 0.6 (0.022)2.75 SPL27506X — SPL27512X SPL27515X SPL27520X SPL27525X — 0.6 (0.023)3.00 SPL30006X SPL30010X SPL30012X SPL30015X SPL30020X SPL30025X SPL30030X 0.6 (0.023)3.25 — — SPL32512X SPL32515X SPL32520X — — 0.6 (0.023)3.50 SPL35006X SPL35010X SPL35012X SPL35015X SPL35020X SPL35025X SPL35030X 0.6 (0.023)3.75 — — SPL37512X SPL37515X SPL37520X — — 0.6 (0.023)4.00 SPL40006X SPL40010X SPL40012X SPL40015X SPL40020X SPL40025X SPL40030X 0.6 (0.024)

Nominal pressure: the pressure at which the balloon reaches its labeled diameter Rated burst pressure: the maximum pressure to which a balloon is designed to be inflated (95% confidence that 99.9% will not fail below rated burst pressure)

Rated burst pressure— do not exceed.Nominal pressure and rated burst pressure are the same.

Sprinter Legend RX Ordering Information

Sprinter Legend Compliance

Proximal shaft (oval)

Distal shaft

Dura-Trac hydrophilic coating

Flexible FasTrac tip design

Platinum iridiummarker bands

Proximal shaft

Distal shaft


Gold-swaged marker bands

Fulcrum® balloon material

Flexible FasTrac tip

Over-the-wire luer

RX luer

Sprinter Legend OTw Ordering Information


Balloon Length (mm) Crossing Profile O.D. mm (in.)6 10 15 20

1.25 SPL12506WL SPL12510WL SPL12515WL SPL12520WL 0.5 (0.020)

Test data on file at Medtronic, Inc.

Nominal pressure.


Balloon Dilatation Catheters

TECHNICAL INFORMATIONCatheter length RX 142 cm; OTW 152 cmDistal shaft length RX 21 cmPlatinum iridium marker bands 1.25–1.50 mm Single 2.00–4.00 mm DoubleDura-Trac selective coatingMiniWrap 1.25 mm Zerofold 1.50 mm 2 folds 2.00–3.75 mm 3 folds 4.00 mm 5 folds

Shaft O.D. for 1.25–3.50 mm Proximal RX 1.9 F; OTW 3.2 F Distal 2.4 F/2.6 FShaft O.D. for 3.75–4.00 mm Proximal RX 1.9 F; OTW 3.2 F Distal 2.5 F/2.7 FMGCID 1.4 mm/.056"

12

C O R O N A R YBalloon Dilatation Catheters

Nominal pressure

Rated burst pressure†

Balloon Diameter

(mm)

Balloon Length (mm) Crossing Profile O.D.

mm (in.)6 10 12 15 20

1.25 SPL12506X SPL12510X SPL12512X SPL12515X SPL12520X 0.5 (0.020)


Test data on file at Medtronic, Inc.†Rated burst pressure—do not exceed.

Nominal pressure and rated burst pressure are the same.

Sprinter Legend 1.25 mm RX Ordering Information

Sprinter Legend 1.25 Compliance

Proximal shaft

Distal shaft


Flexible FasTrac tip design

Platinum iridiummarker band

Proximal shaft

Distal shaft



Fulcrum® balloon material


Over-the-wire

Sprinter Legend 1.25 mm OTw Ordering InformationBalloon

Diameter (mm)

Balloon Length (mm) Crossing Profile O.D.

mm (in.)6 10 15 20

1.25 SPL12506WL SPL12510WL SPL12515WL SPL12520WL 0.5 (0.020)

Pressure(atm)

Deployed Stent I.D. (mm)

1.254 0.605 0.606 0.637 0.678 0.759 0.86

10 0.9911 1.1112 1.2013 1.2814 1.3515 1.4016 —

Product Description:

The Sprinter Legend 1.25-mm semi–compliant balloon dilatation catheter with award-winning* SuperCrosser Zerofold Technology.

The Lowest Crossing Profile on the Market‡

Lesion entry profile: 0.41 mm (0.016")Crossing profile: 0.5 mm (0.020")Profile over mid-marker: 0.6 mm (0.024")

‡ In testing vs. US competitors. Test data on file at Medtronic, Inc. Bench testing may not be indicative of clinical performance.

* Medtronic CardioVascular in Ireland was selected as the overall winner of the Innovation Company of the Year Award 2007 for its SuperCrosser Zerofold Technology by The Institution of Engineers of Ireland.

Sprinter® Legend 1.25 mm Semicompliant Balloon Dilatation Catheter

0.41-mm (0.016")FasTrac tapered tip

Micro-Britelow-profile marker band

SuperCrosser Zerofold Technology(no balloon wrap or shoulders)

0.5-mm (0.020")crossing profile

TECHNICAL INFORMATIONCatheter length RX 142 cm; OTW 152 cmDistal shaft length RX 21 cmPlatinum iridium marker bands 1.25 mm SingleDura-Trac selective coatingMiniWrap 1.25 mm ZerofoldShaft dimensions for 1.25 mm Proximal RX 1.9 F; OTW 3.2 F Distal 2.4 F/2.6 FMGCID 1.4 mm/.056”



13


Sprinter® OTw Semicompliant Balloon Dilatation Catheter

Sprinter OTw Ordering Information

Sprinter OTw Compliance


Balloon Length (mm) Crossing Profile O.D. mm (in.)6 10 12 15 20 25 30

1.50 SPR1506W SPR1510W SPR1512W SPR1515W SPR1520W — — 0.53 (0.021)2.00 SPR2006W SPR2010W SPR2012W SPR2015W SPR2020W SPR2025W SPR2030W 0.56 (0.022)2.25 SPR22506W — SPR22512W SPR22515W SPR22520W — — 0.56 (0.022)2.50 SPR2506W SPR2510W SPR2512W SPR2515W SPR2520W SPR2525W SPR2530W 0.58 (0.023)2.75 SPR27506W — SPR27512W SPR27515W SPR27520W — — 0.58 (0.023)3.00 SPR3006W SPR3010W SPR3012W SPR3015W SPR3020W SPR3025W SPR3030W 0.58 (0.023)3.25 — — SPR32512W SPR32515W SPR32520W — — 0.58 (0.023)3.50 SPR3506W SPR3510W SPR3512W SPR3515W SPR3520W SPR3525W SPR3530W 0.58 (0.023)3.75 — — SPR37512W SPR37515W SPR37520W — — 0.58 (0.023)4.00 SPR4006W SPR4010W SPR4012W SPR4015W SPR4020W SPR4025W SPR4030W 0.60 (0.024)

TECHNICAL INFORMATIONCatheter length 138 cmGold-swaged marker bands 1.5 mm Single 2.00–4.00 mm DoubleDura-Trac selective coatingFulcrum® balloon materialMiniWrap 1.5 mm 2 folds 2.0–3.75 mm 3 folds 4.0 mm 5 folds

Nominal pressure: the pressure at which the balloon reaches its labeled diameter. Rated burst pressure: the maximum pressure to which a balloon is designed to be inflated (95% con-fidence that 99.9% will not fail below rated burst pressure).

Pressure(atm)

Balloon Diameter (mm)1.50 2.00 2.25 2.50 2.75 3.00 3.25 3.50 3.75 4.00

4 1.40 1.79 2.00 2.21 2.43 2.65 2.88 3.11 3.31 3.515 1.45 1.85 2.07 2.29 2.52 2.75 2.99 3.23 3.44 3.666 1.50 1.91 2.14 2.36 2.62 2.87 3.10 3.33 3.55 3.787 1.55 1.96 2.20 2.44 2.69 2.94 3.18 3.41 3.66 3.918 1.58 2.00 2.25 2.50 2.75 3.00 3.25 3.50 3.75 4.009 1.61 2.04 2.29 2.55 2.80 3.06 3.31 3.56 3.82 4.08

10 1.63 2.07 2.33 2.59 2.84 3.10 3.36 3.62 3.88 4.1511 1.66 2.10 2.36 2.62 2.89 3.15 3.41 3.66 3.94 4.2112 1.68 2.12 2.39 2.66 2.92 3.18 3.44 3.71 3.99 4.2613 1.70 2.15 2.42 2.69 2.96 3.23 3.49 3.75 4.03 4.3114 1.72 2.18 2.45 2.72 2.99 3.27 3.54 3.80 4.08 4.3615 1.75 2.20 2.47 2.74 3.03 3.32 3.59 3.86 4.14 4.4216 — 2.22 2.50 2.78 3.07 3.36 3.63 3.91 4.19 4.4717 — 2.25 2.53 2.81 3.10 3.40 3.68 3.96 4.24 4.5218 — 2.28 2.56 2.84 3.15 3.46 3.74 4.02 4.30 4.58


Test data on file at Medtronic, Inc.Bench test results may not be indicative of clinical performance.



Nominal pressure


Shaft dimensions for 1.5–3.5 mm Proximal 3.2 F Distal 2.4 F/2.6 FShaft dimensions for 3.75–4.0 mm Proximal 3.2 F Distal 2.5 FMGCID 0.056"

Proximal shaft

Distal shaft




Fulcrum balloon material

14


NC Sprinter® RX Noncompliant Balloon Dilatation Catheter

NC Sprinter RX Compliance


Proximal shaftGold-swagedmarker bands

Distal shaft

Dura-Trachydrophiliccoating

Soft Fulcrum Plusballoon material

NC Sprinter RX Ordering Information

TECHNICAL INFORMATIONCatheter length 142 cmGold-swaged marker bands 2.00–5.00 mm DoubleDura-Trac selective coatingSoft Fulcrum Plus balloon materialMiniWrap 2.00–3.75 mm 3 folds 4.00–5.00 mm 5 foldsShaft dimensions for 2.00–3.75 mm Proximal 0.65 mm (1.9 F) Distal 0.81 mm/0.86 mm (2.4 F/2.6 F)


Balloon Length (mm) Crossing Profile O.D. mm (in.)6 9 12 15 21 27

2.00 NCSP2006X NCSP2009X NCSP2012X NCSP2015X NCSP2021X — 0.60 (0.024)2.25 NCSP22506X — NCSP22512X — NCSP22521X — 0.62 (0.024)2.50 NCSP2506X NCSP2509X NCSP2512X NCSP2515X NCSP2521X NCSP2527X 0.63 (0.025)2.75 NCSP27506X — NCSP27512X NCSP27515X NCSP27521X — 0.65 (0.025)3.00 NCSP3006X NCSP3009X NCSP3012X NCSP3015X NCSP3021X NCSP3027X 0.66 (0.026)3.25 NCSP32506X NCSP32509X NCSP32512X NCSP32515X NCSP32521X — 0.68 (0.027)3.50 NCSP3506X NCSP3509X NCSP3512X NCSP3515X NCSP3521X NCSP3527X 0.70 (0.027)3.75 NCSP37506X NCSP37509X NCSP37512X NCSP37515X NCSP37521X — 0.71 (0.028)4.00 NCSP4006X NCSP4009X NCSP4012X NCSP4015X NCSP4021X NCSP4027X 0.73 (0.029)4.50 — — — NCSP4515X NCSP4521X — 0.76 (0.030)5.00 — — — NCSP5015X — — 0.80 (0.032)

Pressure(atm)

Balloon Diameter (mm)2.00 2.25 2.50 2.75 3.00 3.25 3.50 3.75 4.00 4.50 5.00

8 1.98 2.17 2.45 2.70 2.97 3.09 3.36 3.62 3.87 4.27 4.759 2.00 2.20 2.49 2.74 3.01 3.15 3.42 3.68 3.93 4.34 4.84

10 2.02 2.23 2.51 2.77 3.04 3.18 3.45 3.72 3.97 4.39 4.9111 2.03 2.24 2.53 2.80 3.07 3.22 3.49 3.76 4.01 4.44 4.9712 2.05 2.26 2.55 2.82 3.10 3.25 3.52 3.79 4.05 4.48 5.0113 2.07 2.28 2.57 2.84 3.13 3.28 3.55 3.82 4.08 4.51 5.0614 2.08 2.30 2.58 2.87 3.15 3.31 3.58 3.85 4.11 4.55 5.1015 2.10 2.32 2.60 2.89 3.18 3.33 3.61 3.88 4.15 4.58 5.1416 2.12 2.33 2.62 2.91 3.20 3.36 3.63 3.90 4.18 4.61 5.1817 2.13 2.36 2.63 2.93 3.23 3.39 3.65 3.93 4.22 4.65 5.2218 2.15 2.38 2.65 2.95 3.26 3.41 3.68 3.96 4.25 4.68 5.2619 2.17 2.40 2.66 2.98 3.29 3.44 3.71 3.99 4.29 4.72 5.30 20 2.19 2.42 2.68 3.00 — 3.47 3.73 4.02 — 4.76 —21 2.21 2.44 2.70 3.03 — 3.50 3.77 4.05 — 4.80 —22 2.23 2.46 2.72 3.05 — 3.53 — 4.08 — 4.84 —






Nominal pressure


Shaft dimensions for 4.00–5.00 mm Proximal 0.65 mm (1.9 F) Distal 1.02 mm (3.0 F)MGCID 1.42 mm/.056" (2.00–4.00 mm)MGCID 1.68 mm/0.066" (4.50–5.00 mm)

15


NC Stormer® OTw Noncompliant Balloon Dilatation Catheter

Tapered tip design


Swaged marker bands

Fulcrum Plus balloon material

Proximal shaftIntermediate shaft

Distal shaft

NC Stormer OTw Compliance

TECHNICAL INFORMATIONNominal pressure 2.0–4.0 mm 10 atmRated burst pressure 2.0–4.0 mm 18 atmCatheter length 138 cmDistal/mid shaft O.D. Distal = 2.5 F Mid = 2.7 F Proximal = 3.2 FExit markers

Brachial, 88 cm Femoral, 98 cm Marker bands 2 on all 2.0–4.0 mm O.D.s

NC Stormer OTw Ordering Information


Balloon Length (mm)6 11 14 16 18 21 26 31

2.00 NCS2006W NCS2011W — NCS2016W — NCS2021W — —2.25 NCS22506W NCS22511W — NCS22516W — NCS22521W — —2.50 NCS2506W NCS2511W NCS2514W NCS2516W NCS2518W NCS2521W — NCS2531W2.75 NCS27506W NCS27511W NCS27514W NCS27516W NCS27518W NCS27521W — —3.00 NCS3006W NCS3011W NCS3014W NCS3016W NCS3018W NCS3021W NCS3026W NCS3031W3.25 NCS32506W NCS32511W NCS32514W NCS32516W NCS32518W NCS32521W — —3.50 NCS3506W NCS3511W NCS3514W NCS3516W NCS3518W NCS3521W NCS3526W —3.75 NCS37506W NCS37511W NCS37514W NCS37516W NCS37518W NCS37521W — —4.00 NCS4006W NCS4011W NCS4014W NCS4016W NCS4018W NCS4021W — —




Dura-Trac selective coatingSoft Fulcrum Plus balloon materialNo. of balloon folds 2.0–2.5 mm O.D.s 3 folds 2.75–3.0 mm O.D.s 4 folds 3.25–3.5 mm O.D.s 5 folds 3.75–4.0 mm O.D.s 6 folds




Nominal pressure

16


17

Coronary Guide Catheters

*Tospecifysideholes,add“SH”totheendoftheproductcode.

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.090 in.)

without Sideholes without Sideholes* without Sideholes* without Sideholes*

JL3.0 LA5JL30 LA6JL30 LA7JL30 LA8JL30






JCL3.0 LA5JCL30 LA6JCL30 LA7JCL30 LA8JCL30





Left Standard

JCL3.5

JCL4.0

JCL3.0

JCL4.5

JCL5.0

JL3.0

JL4.0

JL5.0

JL6.0JL3.5

JL4.5

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.090 in.)


SL3.0 LA5SL30 LA6SL30 LA7SL30 LA8SL30






Short Left SL3.0

SL3.5

SL4.0

SL4.5

SL5.0

SL6.0

Launcher® Guide Catheters LEFT CORONARY CURVES


For distribution in the USA only.© 2011 Medtronic, Inc. All rights reserved. UC200104300fEN 8/11

18For distribution in the USA only.

© 2011 Medtronic, Inc. All rights reserved. UC200104300fEN 8/11

C O R O N A R YGuide Catheters

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.090 in.)


AL.75 LA5AL75 LA6AL75 LA7AL75 LA8AL75AL1.0 LA5AL10 LA6AL10 LA7AL10 LA8AL10AL1.5 LA5AL15 LA6AL15 LA7AL15 LA8AL15AL2.0 LA5AL20 LA6AL20 LA7AL20 LA8AL20AL2.5 LA5AL25 LA6AL25 LA7AL25 LA8AL25AL3.0 LA5AL30 LA6AL30 LA7AL30 LA8AL30AL4.0 LA5AL40 LA6AL40 LA7AL40 LA8AL40

Amplatz Left

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.090 in.)


SAL.75 LA5SAL75 LA6SAL75 LA7SAL75 LA8SAL75SAL1.0 LA5SAL10 LA6SAL10 LA7SAL10 LA8SAL10SAL1.5 LA5SAL15 LA6SAL15 LA7SAL15 LA8SAL15SAL2.0 LA5SAL20 LA6SAL20 LA7SAL20 LA8SAL20SAL2.5 LA5SAL25 LA6SAL25 LA7SAL25 LA8SAL25SAL3.0 LA5SAL30 LA6SAL30 LA7SAL30 LA8SAL30SAL4.0 LA5SAL40 LA6SAL40 LA7SAL40 LA8SAL40

Short Amplatz Left

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.090 in.)


EBU3.0 LA5EBU30 LA6EBU30 LA7EBU30 LA8EBU30EBU3.5 LA5EBU35 LA6EBU35 LA7EBU35 LA8EBU35

EBU3.75 LA5EBU375 LA6EBU375 LA7EBU375 LA8EBU375EBU4.0 LA5EBU40 LA6EBU40 LA7EBU40 LA8EBU40EBU4.5 LA5EBU45 LA6EBU45 LA7EBU45 LA8EBU45EBU5.0 LA5EBU50 LA6EBU50 LA7EBU50 LA8EBU50

Left Backup Support

EBU (Extra Backup)

AL2.0

AL1.0

AL1.5

AL.75

AL2.5

AL3.0

AL4.0

SAL.75

SAL1.0

SAL1.5

SAL2.0 SAL3.0

SAL4.0SAL2.5

EBU3.0

EBU3.5

EBU3.75

EBU5.0EBU4.0

EBU4.5


Launcher left coronary curves, continued




Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.090 in.)


JR3.0 LA5JR30 LA6JR30 LA7JR30 LA8JR30JR3.5 LA5JR35 LA6JR35 LA7JR35 LA8JR35JR4.0 LA5JR40 LA6JR40 LA7JR40 LA8JR40JR4.5 LA5JR45 LA6JR45 LA7JR45 LA8JR45JR5.0 LA5JR50 LA6JR50 LA7JR50 LA8JR50JR6.0 LA5JR60 LA6JR60 LA7JR60 LA8JR60

JCR3.5 LA5JCR35 LA6JCR35 LA7JCR35 LA8JCR35JCR4.0 LA5JCR40 LA6JCR40 LA7JCR40 LA8JCR40JCR4.5 LA5JCR45 LA6JCR45 LA7JCR45 LA8JCR45JCR5.0 LA5JCR50 LA6JCR50 LA7JCR50 LA8JCR50

Right Standard JR3.0

JR4.0

JR5.0

JR6.0

JR3.5

JR4.5JCR3.5

JCR4.0

JCR4.5

JCR5.0

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.090 in.)


SR3.0 LA5SR30 LA6SR30 LA7SR30 LA8SR30SR3.5 LA5SR35 LA6SR35 LA7SR35 LA8SR35SR4.0 LA5SR40 LA6SR40 LA7SR40 LA8SR40SR4.5 LA5SR45 LA6SR45 LA7SR45 LA8SR45SR5.0 LA5SR50 LA6SR50 LA7SR50 LA8SR50SL6.0 LA5SR60 LA6SR60 LA7SR60 LA8SR60

Short Right SR3.0

SR3.5

SR4.0

SR6.0

SR5.0

SR4.5

Amplatz Right

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.090 in.)


AR1.0 LA5AR10 LA6AR10 LA7AR10 LA8AR10AR2.0 LA5AR20 LA6AR20 LA7AR20 LA8AR20

ALR1-2 LA5ALR12† LA6ALR12† LA7ALR12† LA8ALR12†

AR2.0AR1.0 ALR1-2

*Tospecifysideholes,add“SH”totheendoftheproductcode.†Specialty curve for extra backup.

General Characteristics:Supplied sterile.items per box: 1Launcher Guide Catheters

RIGHT CORONARY CURVES




Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.090 in.)


SCR3.5 LA5SCR35 LA6SCR35 LA7SCR35 LA8SCR35SCR4.0 LA5SCR40 LA6SCR40 LA7SCR40 LA8SCR40SCR5.0 LA5SCR50 LA6SCR50 LA7SCR50 LA8SCR50

SCR3.5 SCR4.0 SCR5.0Shepherd’s Crook Right

ECR3.5

ECR3.0 ECR4.5ECR4.0ECR

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.090 in.)


ECR3.5 LA5ECR35 LA6ECR35 LA7ECR35 LA8ECR35ECR4.0 LA5ECR40 LA6ECR40 LA7ECR40 LA8ECR40ECR4.5 LA5ECR45 LA6ECR45 LA7ECR45 LA8ECR45

RBUNOTO3DRC3DRIGHT

RBU 3.5

RBU 4.0

RBU 4.5

NOTO

3DRC

3DRIGHT

Right Backup Support

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.090 in.)


RBU3.5 LA5RBU35 LA6RBU35 LA7RBU35 LA8RBU35RBU4.0 LA5RBU40 LA6RBU40 LA7RBU40 LA8RBU40RBU4.5 — LA6RBU45 — —NOTO LA5NOTO LA6NOTO LA7NOTO LA8NOTO3DRC — LA63DRC LA73DRC LA83DRC

3DRIGHT LA53DRIGHT LA63DRIGHT — —

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.090 in.)


SAR1.0 LA5SAR10 LA6SAR10 LA7SAR10 LA8SAR10SAR2.0 LA5SAR20 LA6SAR20 LA7SAR20 LA8SAR20

SAR2.0SAR1.0Short Amplatz Right


Launcher right coronary curves, continued




Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

without Sideholes without Sideholes

MRADIAL LA5MRADIAL LA6MRADIALMRESS LA5MRESS LA6MRESSRRAD LA5RRAD LA6RRADLARA LA5LARA LA6LARA

Radial Curves

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)


EBU

LA5EBU30 LA6EBU30LA5EBU35 LA6EBU35

LA5EBU375 LA6EBU375LA5EBU40 LA6EBU40LA5EBU45 LA6EBU45LA5EBU50 LA6EBU50

ALR12 LA5ALR12 LA6ALR12

MAC

LA5MAC30 LA6MAC30LA5MAC35 LA6MAC35

LA5MAC375 LA6MAC375LA5MAC40 LA6MAC40LA5MAC45 LA6MAC45

MRADIAL

MRESS

LARA

RRAD

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)


MAC3030 LA5MAC3030 LA6MAC3030

HOCKEYSTICK

LA5HSI LA6HSILA5HSII LA6HSII

LA5HSREL LA6HSRELLA5HSIII LA6HSIII

MULTIPURPOSE LA5MPST LA6MPSTIMA LA5IMA LA6IMA

Other Launcher curves that can be used for transradial procedures

Curve StyleRecommended Sizing

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

Artery without Sideholes without Sideholes

ERADL Left main, standard-size aorta LA5ERADL LA6ERADLERADLLT Left main, enlarged aorta LA5ERADLLT LA6ERADLLTERADLST Left main, narrowed aorta LA5ERADLST LA6ERADLSTERADR Right coronary artery, standard-size aorta LA5ERADR LA6ERADR

ERADRST Right coronary artery, narrowed aorta LA5ERADRST LA6ERADRST

erADL easy radial Left

erADLSteasy radial Left Short tip

erADreasy radial right

erADrSteasy radial right Short tip

erADLLteasy radial Left Long tip

Easy RadialERADL

Launcher Guide Catheters RADIAL CURVES





MultipurposeMB1

MP1

MB2

MPST

Hockey Stick II

Hockey Stick III

El Gamal

Hockey Stick Relaxed

Hockey Stick I

MP2

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.090 in.)


MB1 LA5MB1 LA6MB1 LA7MB1 LA8MB1

MB2 LA5MB2 LA6MB2 LA7MB2 LA8MB2

MP1 LA5MP1 LA6MP1 LA7MP1 LA8MP1

MP2 — LA6MP2 — —

MPST LA5MPST LA6MPST LA7MPST LA8MPST

HockeyStickI LA5HSI LA6HSI LA7HSI LA8HSI

HockeyStickII LA5HSII LA6HSII LA7HSII LA8HSII

HockeyStickRelaxed LA5HSREL LA6HSREL LA7HSREL LA8HSREL

HockeyStickIII LA5HSIII LA6HSIII LA7HSIII LA8HSIII

El Gamal LA5ELGAMAL LA6ELGAMAL LA7ELGAMAL LA8ELGAMAL

MAC(Multi-Aortic)

MAC3.0

MAC3.5

MAC3.75

MAC4.0

MAC4.5

MAC5.0

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.090 in.)


MAC3.0 LA5MAC30 LA6MAC30 LA7MAC30 LA8MAC30







Launcher Guide CathetersOTHER CURVES





Bypass Curves LCB

RCB

IMARCBII

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.090 in.)


LCB LA5LCB LA6LCB LA7LCB LA8LCB

LCB (90 cm) — LA7LCBD LA7LCBD LA8LCBD

RCB LA5RCB LA6RCB LA7RCB LA8RCB

RCB (90 cm) LA5RCBD LA6RCBD LA7RCBD LA8RCBD

RCBII LA5RCBII LA6RCBII LA7RCBII LA8RCBII

IMA LA5IMA LA6IMA LA7IMA LA8IMA

IMA (90 cm) LA5IMAD LA6IMAD LA7IMAD LA8IMAD

Champ Champ0.5

Champ1.5

Champ1.0

Champ2.0

Champ2.5

Champ3.0

Champ3.5

Champ4.0

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.071 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.090 in.)


Champ0.5 LA5CHAMP05 LA6CHAMP05 LA7CHAMP05 LA8CHAMP05









Launcher—other curves, continued


© 2011 Medtronic, Inc. All rights reserved. UC200805222aEN 8/11


Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

without Sideholes without Sideholes with Sideholes

JL3.0 SA5JL30 SA6JL30 SA6JL30SH






JCL3.0 SA5JCL30 SA6JCL30 SA6JCL30SH





Left Standard

JCL3.5

JCL4.0

JCL3.0

JCL4.5

JCL5.0

JL3.0

JL4.0

JL5.0

JL6.0JL3.5

JL4.5

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


SL3.0 SA5SL30 SA6SL30 SA6SL30SH






Short LeftSL3.0

SL3.5

SL4.0

SL4.5

SL5.0

SL6.0


Sherpa NX Active Guide CathetersLEFT CORONARY CURVES




Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


SAL.75 SA5SAL75 SA6SAL75 SA6SAL75SHSAL1.0 SA5SAL10 SA6SAL10 SA6SAL10SHSAL1.5 SA5SAL15 SA6SAL15 SA6SAL15SHSAL2.0 SA5SAL20 SA6SAL20 SA6SAL20SHSAL2.5 SA5SAL25 SA6SAL25 SA6SAL25SHSAL3.0 SA5SAL30 SA6SAL30 SA6SAL30SHSAL4.0 SA5SAL40 SA6SAL40 SA6SAL40SH

Short Amplatz Left

SAL.75

SAL1.0

SAL1.5

SAL2.0 SAL3.0

SAL4.0SAL2.5

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


AL.75 SA5AL75 SA6AL75 SA6AL75SHAL1.0 SA5AL10 SA6AL10 SA6AL10SHAL1.5 SA5AL15 SA6AL15 SA6AL15SHAL2.0 SA5AL20 SA6AL20 SA6AL20SHAL2.5 SA5AL25 SA6AL25 SA6AL25SHAL3.0 SA5AL30 SA6AL30 SA6AL30SHAL4.0 SA5AL40 SA6AL40 SA6AL40SH

Amplatz Left AL2.0

AL1.0

AL1.5

AL.75

AL2.5

AL3.0

AL4.0

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


EBU3.0 SA5EBU30 SA6EBU30 SA6EBU30SHEBU3.5 SA5EBU35 SA6EBU35 SA6EBU35SH

EBU3.75 SA5EBU375 SA6EBU375 SA6EBU375SHEBU4.0 SA5EBU40 SA6EBU40 SA6EBU40SHEBU4.5 SA5EBU45 SA6EBU45 SA6EBU45SHEBU5.0 SA5EBU50 SA6EBU50 SA6EBU50SH

LeftBackup Support

EBU (Extra Backup)

EBU3.0

EBU3.5

EBU3.75

EBU5.0EBU4.0

EBU4.5

Sherpa nX Active left coronary curves, continued




Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


JR3.0 SA5JR30 SA6JR30 SA6JR30SHJR3.5 SA5JR35 SA6JR35 SA6JR35SHJR4.0 SA5JR40 SA6JR40 SA6JR40SHJR4.5 SA5JR45 SA6JR45 SA6JR45SHJR5.0 SA5JR50 SA6JR50 SA6JR50SHJR6.0 SA5JR60 SA6JR60 SA6JR60SH

JCR3.5 SA5JCR35 SA6JCR35 SA6JCR35SHJCR4.0 SA5JCR40 SA6JCR40 SA6JCR40SHJCR4.5 SA5JCR45 SA6JCR45 SA6JCR45SHJCR5.0 SA5JCR50 SA6JCR50 SA6JCR50SH

JR3.0

JR4.0

JR5.0

JR6.0

JR3.5

JR4.5JCR3.5

JCR4.0

JCR4.5

JCR5.0

Right Standard

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


SR3.0 SA5SR30 SA6SR30 SA6SR30SHSR3.5 SA5SR35 SA6SR35 SA6SR35SHSR4.0 SA5SR40 SA6SR40 SA6SR40SHSR4.5 SA5SR45 SA6SR45 SA6SR45SHSR5.0 SA5SR50 SA6SR50 SA6SR50SHSL6.0 SA5SR60 SA6SR60 SA6SR60SH

SR3.0

SR3.5

SR4.0

SR6.0

SR5.0

SR4.5

Short Right

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


AR1.0 SA5AR10 SA6AR10 SA6AR10SHAR2.0 SA5AR20 SA6AR20 SA6AR20SH

ALR1-2 SA5AR12 SA6ALR12 SA6ALR12SH

AR2.0AR1.0 ALR1-2Amplatz Right

Sherpa NX Active RIGHT CORONARY CURVES





Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


SCR3.5 SA5SCR35 SA6SCR35 SA6SCR35SHSCR4.0 SA5SCR40 SA6SCR40 SA6SCR40SHSCR5.0 SA5SCR50 SA6SCR50 SA6SCR50SH


Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


ECR3.0 — SA6ECR30 SA6ECR30SHECR3.5 SA5ECR35 SA6ECR35 SA6ECR35SHECR4.0 SA5ECR40 SA6ECR40 SA6ECR40SHECR4.5 SA5ECR45 SA6ECR45 SA6ECR45SH

ECR3.5

ECR3.0 ECR4.5ECR4.0RightBackupSupport

ECR

RBUNOTO3DRC3DRIGHT

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


RBU3.5 SA5RBU35 SA6RBU35 SA6RBU35SHRBU4.0 SA5RBU40 SA6RBU40 SA6RBU40SHRBU4.5 — SA6RBU45 SA6RBU45SHNOTO SA5NOTO SA6NOTO SA6NOTOSH

3DRIGHT SA53DRIGHT SA63DRIGHT SA63DRIGHTSH3DRC — SA63DRC SA63DRCSH

RBU 3.5

RBU 4.0

RBU 4.5

3DRIGHT

NOTO

3DRC

Backup Support

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


SAR1.0 SA5SAR10 SA6SAR10 SA6SAR10SHSAR2.0 SA5SAR20 SA6SAR20 SA6SAR20SH

SAR1.0 SAR2.0Short Amplatz Right

Sherpa nX Active right coronary curves, continued




Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


EBU

SA5EBU30 SA6EBU30SA5EBU35 SA6EBU35

SA5EBU375 SA6EBU375SA5EBU40 SA6EBU40SA5EBU45 SA6EBU45SA5EBU50 SA6EBU50

ALR12 SA5ALR12 SA6ALR12

MAC

SA5MAC30 SA6MAC30SA5MAC35 SA6MAC35

SA5MAC375 SA6MAC375SA5MAC40 SA6MAC40SA5MAC45 SA6MAC45

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


MRADIAL SA5MRADIAL SA6MRADIALMRESS SA5MRESS SA6MRESS

RRADIAL SA5RRAD SA6RRADLARA SA5LARA SA6LARA

Radial Curves

MRADIAL

MRESS

LARA

RRAD

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

without Sideholes without SideholesMAC3030 SA5MAC3030 SA6MAC3030

HOCKEYSTICK

SA5HSI SA6HSISA5HSII SA6HSII

SA5RMHSII SA6RMHSIISA5HSIII SA6HSIII

MULTIPURPOSE SA5MPST SA6MPSTIMA SA5IMA SA6IMA

Other Sherpa NX Active curves that can be used for transradial procedures


5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

Artery without Sideholes without Sideholes

ERADL Left main, standard-size aorta SA5ERADL SA6ERADLERADLLT Left main, enlarged aorta SA5ERADLLT SA6ERADLLTERADLST Left main, narrowed aorta SA5ERADLST SA6ERADLSTERADR Right coronary artery, standard-size aorta SA5ERADR SA6ERADR

ERADRST Right coronary artery, narrowed aorta SA5ERADRST SA6ERADRST






Easy Radial

Sherpa NX Active RADIAL CURVES





MAC(Multi-Aortic)

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


MAC3.0 SA5MAC30 SA6MAC30 SA6MAC30SHMAC3.5 SA5MAC35 SA6MAC35 SA6MAC35SH

MAC3.75 SA5MAC375 SA6MAC375 SA6MAC375SHMAC4.0 SA5MAC40 SA6MAC40 SA6MAC40SHMAC4.5 SA5MAC45 SA6MAC45 SA6MAC45SHMAC5.0 SA5MAC50 SA6MAC50 SA6MAC50SH

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


MB1.0 SA5MB1 SA6MB1 SA6MB1SHMB2.0 SA5MB2 SA6MB2 SA6MB2SHMP1 SA5MP1 SA6MP1 SA6MP1SHMP2 — SA6MP2 SA6MP2SH

MPST SA5MPST SA6MPST —HockeyStickI SA5HSI SA6HSI SA6HSISHHockeyStickII SA5HSII SA6HSII SA6HSIISH

HockeyStickRelaxed SA5HSREL SA6HSREL SA6HSRELSHHockeyStickIII SA5HSIII SA6HSIII SA6HSIIISH

El Gamal SA5ELGAMAL SA6ELGAMAL SA6ELGAMALSH

Multipurpose

MP1

MB1

MB2

MPST

Hockey Stick II

Hockey Stick III

El Gamal


Hockey Stick I

MAC3.0

MAC3.5

MAC3.75

MAC4.0

MAC4.5

MAC5.0

Sherpa NX Active OTHER CURVES





Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


Champ0.5 SA5CHAMP05 SA6CHAMP05 SA6CHAMP05SH








Champ Champ0.5

Champ1.5

Champ1.0

Champ2.0

Champ2.5

Champ3.0

Champ3.5

Champ4.0

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)


LCB SA5LCB SA6LCB SA6LCBSH

LCB (90 cm) — SA6LCBD SA6LCBDSH

RCB SA5RCB SA6RCB SA6RCBSH

RCB (90 cm) SA5RCBD SA6RCBD SA6RCBDSH

RCBII SA5RCBII SA6RCBII SA6RCBIISH

IMA SA5IMA SA6IMA SA6IMASH

IMA (90 cm) SA5IMAD SA6IMAD SA6IMADSH

Bypass Curves LCB

RCB

IMARCBII

Sherpa nX Active—other curves, continued




Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

8 F(i.D. 0.088 in.)

without Sideholes* without Sideholes* without Sideholes*

SL3.0 SB6SL30 SB7SL30 SB8SL30SL3.5 SB6SL35 SB7SL35 SB8SL35SL4.0 SB6SL40 SB7SL40 SB8SL40SL4.5 SB6SL45 SB7SL45 SB8SL45SL5.0 SB6SL50 SB7SL50 SB8SL50SL6.0 SB6SL60 SB7SL60 SB8SL60

Short Left

*Tospecifysideholes,add“SH”toproductcode.

Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

8 F(i.D. 0.088 in.)


JL3.0 SB6JL30 SB6JL30 SB6JL30






JCL3.0 SB6JCL30 SB6JCL30 SB6JCL30





Left Standard

JCL3.5

JCL4.0

JCL3.0

JCL4.5

JCL5.0

JL3.0

JL4.0

JL5.0

JL6.0JL3.5

JL4.5

SL3.0

SL3.5

SL4.0

SL4.5

SL5.0

SL6.0


Sherpa NX Balanced Guide Catheters LEFT CORONARY CURVES




Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

8 F(i.D. 0.088 in.)


AL.75 SB6AL75 SB7AL75 SB8AL75AL1.0 SB6AL10 SB7AL10 SB8AL10AL1.5 SB6AL15 SB7AL15 SB8AL15AL2.0 SB6AL20 SB7AL20 SB8AL20AL2.5 SB6AL25 SB7AL25 SB8AL25AL3.0 SB6AL30 SB7AL30 SB8AL30AL4.0 SB6AL40 SB7AL40 SB8AL40

Amplatz Left AL2.0

AL1.0

AL1.5

AL.75

AL2.5

AL3.0

AL4.0

Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

8 F(i.D. 0.088 in.)


SAL.75 SB6SAL75 SB7SAL75 SB8SAL75SAL1.0 SB6SAL10 SB7SAL10 SB8SAL10SAL1.5 SB6SAL15 SB7SAL15 SB8SAL15SAL2.0 SB6SAL20 SB7SAL20 SB8SAL20SAL2.5 SB6SAL25 SB7SAL25 SB8SAL25SAL3.0 SB6SAL30 SB7SAL30 SB8SAL30SAL4.0 SB6SAL40 SB7SAL40 SB8SAL40

Short Amplatz Left

SAL.75

SAL1.0

SAL1.5

SAL2.0 SAL3.0

SAL4.0SAL2.5

Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

8 F(i.D. 0.088 in.)


EBU3.0 SB6EBU30 SB7EBU30 SB8EBU30EBU3.5 SB6EBU35 SB7EBU35 SB8EBU35

EBU3.75 SB6EBU375 SB7EBU375 SB8EBU375EBU4.0 SB6EBU40 SB7EBU40 SB8EBU40EBU4.5 SB6EBU45 SB7EBU45 SB8EBU45EBU5.0 SB6EBU50 SB7EBU50 SB8EBU50

Backup Support Left

EBU (Extra Backup)

EBU3.0

EBU3.5

EBU3.75

EBU5.0EBU4.0

EBU4.5


Sherpa nX Balanced left coronary curves, continued




Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

8 F(i.D. 0.088 in.)


JR3.0 SB6JR30 SB7JR30 SB8JR30JR3.5 SB6JR35 SB7JR35 SB8JR35JR4.0 SB6JR40 SB7JR40 SB8JR40JR4.5 SB6JR45 SB7JR45 SB8JR45JR5.0 SB6JR50 SB7JR50 SB8JR50JR6.0 SB6JR60 SB7JR60 SB8JR60

JCR3.5 SB6JCR35 SB7JCR35 SB8JCR35JCR4.0 SB6JCR40 SB7JCR40 SB8JCR40JCR4.5 SB6JCR45 SB7JCR45 SB8JCR45JCR5.0 SB6JCR50 SB7JCR50 SB8JCR50


JR4.0

JR5.0

JR6.0

JR3.5

JR4.5JCR3.5

JCR4.0

JCR4.5

JCR5.0

Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

8 F(i.D. 0.088 in.)


SR3.0 SB6SR30 SB7SR30 SB8SR30SR3.5 SB6SR35 SB7SR35 SB8SR35SR4.0 SB6SR40 SB7SR40 SB8SR40SR4.5 SB6SR45 SB7SR45 SB8SR45SR5.0 SB6SR50 SB7SR50 SB8SR50SL6.0 SB6SR60 SB7SR60 SB8SR60

Short Right SR3.0

SR3.5

SR4.0

SR6.0

SR5.0

SR4.5

AR2.0AR1.0 ALR1-2Amplatz Right

Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

8 F(i.D. 0.088 in.)


AR1.0 SB6SR30 SB7SR30 SB8SR30AR2.0 SB6SR50 SB7SR50 SB8SR50

ALR1-2 SB6SR60 SB7SR60 SB8SR60


Sherpa NX Balanced RIGHT CORONARY CURVES





Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

8 F(i.D. 0.088 in.)


SCR3.5 SB6SCR35 SB7SCR35 SB8SCR35SCR4.0 SB6SCR40 SB7SCR40 SB8SCR40SCR4.5 SB6SCR45 SB7SCR45 SB8SCR45


Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

8 F(i.D. 0.088 in.)


SAR1.0 SB6SAR10 SB7SAR10 SB8SAR10SAR2.0 SB6SAR20 SB7SAR20 SB8SAR20

AR2.0AR1.0 ALR1-2Short Amplatz Right

ECR3.5

ECR3.0 ECR4.5ECR4.0ECR

Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

8 F(i.D. 0.088 in.)


ECR3.0 — SB7ECR30 SB8ECR30SHECR3.5 SB6ECR35 SB7ECR35 SB8ECR35SHECR4.0 SB6ECR40 SB7ECR40 SB8SCR40SHECR4.5 SB6ECR45 SB7ECR45 SB8ECR45SH

RBUNOTO3DRC3DRIGHT

RBU 3.5

RBU 4.0

RBU 4.5

3DRIGHT

NOTO

3DRC


Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

8 F(i.D. 0.088 in.)


RBU3.5 SB6RBU35 SB7RBU35 SB8RBU35RBU4.0 SB6RBU40 SB7RBU40 SB8RBU40RBU4.5 SB6RBU45 SB7RBU45 SB8RBU45NOTO SB6NOTO SB7NOTO SB8NOTO3DRC — SB73DRC SB83DRC

3DRIGHT SB63DRIGHT SB73DRIGHT SB83DRIGHT

Sherpa nX Balanced right coronary curves, continued





Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

without Sideholes without Sideholes*

MRADIAL SB6MRADIAL SB7MRADIALMRESS SB6MRESS SB7MRESSRRAD SB6RRAD SB7RRADLARA SB6LARA SB7LARA

Radial Curves

MRADIAL

MRESS

LARA

RRAD


6 F(i.D. 0.070 in.)

Artery without Sideholes

ERADL Left main, standard-size aorta SB6ERADLERADLLT Left main, enlarged aorta SB6ERADLLTERADLST Left main, narrowed aorta SB6ERADLSTERADR Right coronary artery, standard-size aorta SB6ERADR

ERADRST Right coronary artery, narrowed aorta SB6ERADRST






Easy Radial

CurveStyle

6 F(i.D. 0.070 in.)

without Sideholes

EBU

SA6EBU30SA6EBU35

SA6EBU375SA6EBU40SA6EBU45SA6EBU50

ALR12 SA6ALR12

MAC

SA6MAC30SA6MAC35

SA6MAC375SA6MAC40SA6MAC45

CurveStyle

6 F(i.D. 0.070 in.)

without Sideholes

MAC3030 SA6MAC3030

HOCKEYSTICK

SA6HSISA6HSII

SA6HSRELSA6HSIII

MULTIPURPOSE SA6MPSTIMA SA6IMA

Other Sherpa NX Balanced curves that can be used for transradial procedures

Sideholes available

Sherpa NX Balanced RADIAL CURVES


*To specify sideholes, add“SH”toproductcode.




Multipurpose

MP1

MP2

MB1

MB2

MPST

Hockey Stick II

Hockey Stick III

El Gamal


Hockey Stick I

Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

8 F(i.D. 0.088 in.)


MB1 SB6MB1 SB7MB1 SB8MB1

MB2 SB6MB2 SB7MB2 SB8MB2

MP1 SB6MP1 SB7MP1 SB8MP1

MP2 SB6MP2 — —

MPST SB6MPST SB7MPST SB8MPST

HockeyStickI SB6HSI SB7HSI SB8HSI

HockeyStickII SB6HSII SB7HSII SB8HSII

HockeyStickRelaxed SB6RMHSII SB7RMHSII SB8RMHSII

HockeyStickIII SB6HSIII SB7HSIII SB8HSIII

El Gamal SB6ELGAMAL SB7ELGAMAL SB8ELGAMAL

Sherpa NX Balanced OTHER CURVES


MAC(Multi-Aortic)

MAC3.0

MAC3.5

MAC3.75

MAC4.0

MAC4.5

MAC5.0

Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

8 F(i.D. 0.088 in.)


MAC3.0 SB6MAC30 SB7MAC30 SB8MAC30










Bypass Grafts LCB

RCB

IMARCBII

Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

8 F(i.D. 0.088 in.)


LCB SB6LCB SB7LCB SB8LCB

LCB (90 cm) SB6LCBD — SB8LCBD

RCB SB6RCB SB7RCB SB8RCB

RCB (90 cm) SB6RCBD SB7RCBD SB8RCBD

RCBII SB6RCBII SB7RCBII SB8RCBII

IMA SB6IMA SB7IMA SB8IMA

IMA (90 cm) SB6IMAD SB7IMAD SB8IMAD

Champ Champ0.5

Champ1.5

Champ1.0

Champ2.0

Champ2.5

Champ3.0

Champ3.5

Champ4.0

Curve Style

6 F(i.D. 0.070 in.)

7 F(i.D. 0.080 in.)

8 F(i.D. 0.088 in.)


Champ0.5 SB6CHAMP05 SB7CHAMP05 SB8CHAMP05








Sherpa nX Balanced—other curves, continued




Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.091 in.)


JL3.0 ZM5JL30 Z26JL30 Z27JL30 Z28JL30JL3.5 ZM5JL35 Z26JL35 Z27JL35 Z28JL35JL4.0 ZM5JL40 Z26JL40 Z27JL40 Z28JL40JL4.5 ZM5JL45 Z26JL45 Z27JL45 Z28JL45JL5.0 ZM5JL50 Z26JL50 Z27JL50 Z28JL50JL6.0 ZM5JL60 Z26JL60 Z27JL60 Z28JL60FL3.0 ZM5FL30 Z26FL30 Z27FL30 Z28FL30FL3.5 ZM5FL35 Z26FL35 Z27FL35 Z28FL35FL4.0 ZM5FL40 Z26FL40 Z27FL40 Z28FL40FL4.5 ZM5FL45 Z26FL45 Z27FL45 Z28FL45FL5.0 ZM5FL50 Z26FL50 Z27FL50 Z28FL50FL6.0 ZM5FL60 Z26FL60 Z27FL60 Z28FL60

JCL3.0 ZM5JCL30 Z26JCL30 Z27JCL30 Z28JCL30JCL3.5 ZM5JCL35 Z26JCL35 Z27JCL35 Z28JCL35JCL4.0 ZM5JCL40 Z26JCL40 Z27JCL40 Z28JCL40JCL4.5 ZM5JCL45 Z26JCL45 Z27JCL45 Z28JCL45JCL5.0 ZM5JCL50 Z26JCL50 Z27JCL50 Z28JCL50

Left Standard

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.091 in.)


SL3.0 ZM5SL30 Z26SL30 Z27SL30 Z28SL30SL3.5 ZM5SL35 Z26SL35 Z27SL35 Z28SL35SL4.0 ZM5SL40 Z26SL40 Z27SL40 Z28SL40SL4.5 ZM5SL45 Z26SL45 Z27SL45 Z28SL45SL5.0 ZM5SL50 Z26SL50 Z27SL50 Z28SL50SL6.0 ZM5SL60 Z26SL60 Z27SL60 Z28SL60

Short Left

JL3.0

JL5.0

JL6.0

JL3.5

JL4.5

JCL3.5

JCL4.0

JCL4.5

JCL5.0

JCL3.0

FL6.0

FL5.0

FL4.5

FL4.0

FL3.5

FL3.0

JL4.0

SL3.0

SL3.5

SL4.0

SL4.5

SL5.0

SL6.0


Z2® Guide CathetersLEFT CORONARY CURVES





Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.091 in.)


AL.75 ZM5AL75 Z26AL75 Z27AL75 Z28AL75AL1.0 ZM5AL10 Z26AL10 Z27AL10 Z28AL10AL1.5 ZM5AL15 Z26AL15 Z27AL15 Z28AL15AL2.0 ZM5AL20 Z26AL20 Z27AL20 Z28AL20AL2.5 ZM5AL25 Z26AL25 Z27AL25 Z28AL25AL3.0 ZM5AL30 Z26AL30 Z27AL30 Z28AL30AL4.0 ZM5AL40 Z26AL40 Z27AL40 Z28AL40

Amplatz Left AL2.0

AL1.0

AL1.5

AL.75

AL2.5

AL3.0

AL4.0

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.091 in.)


SAL.75 ZM5SAL75 Z26SAL75 Z27SAL75 Z28SAL75SAL1.0 ZM5SAL10 Z26SAL10 Z27SAL10 Z28SAL10SAL1.5 ZM5SAL15 Z26SAL15 Z27SAL15 Z28SAL15SAL2.0 ZM5SAL20 Z26SAL20 Z27SAL20 Z28SAL20SAL2.5 ZM5SAL25 Z26SAL25 Z27SAL25 Z28SAL25SAL3.0 ZM5SAL30 Z26SAL30 Z27SAL30 Z28SAL30SAL4.0 ZM5SAL40 Z26SAL40 Z27SAL40 Z28SAL40

Short Amplatz Left

SAL.75

SAL1.0

SAL1.5

SAL2.0 SAL3.0

SAL4.0SAL2.5

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.091 in.)


EBU3.0 ZM5EBU30 Z26EBU30 Z27EBU30 Z28EBU30EBU3.5 ZM5EBU35 Z26EBU35 Z27EBU35 Z28EBU35

EBU3.75 ZM5EBU375 Z26EBU375 Z27EBU375 Z28EBU375EBU4.0 ZM5EBU40 Z26EBU40 Z27EBU40 Z28EBU40EBU4.5 ZM5EBU45 Z26EBU45 Z27EBU45 Z28EBU45EBU5.0 ZM5EBU50 Z26EBU50 Z27EBU50 Z28EBU50

Left Backup Support

EBU (Extra Backup)

EBU3.0

EBU3.5

EBU3.75

EBU5.0EBU4.0

EBU4.5


Z2 left coronary curves, continued




Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.091 in.)


JR3.0 ZM5JR30 Z26JR30 Z27JR30 Z28JR30






FR3.0 ZM5FR30 Z26FR30 Z27FR30 Z28FR30






JCR3.5 ZM5JCR35 Z26JCR35 Z27JCR35 Z28JCR35





JR4.0

JR5.0

JR6.0

JR3.5

JR4.5

JCR3.5

JCR4.0

JCR4.5

JCR5.0

FR3.0

FR3.5

FR4.0

FR4.5

FR5.0

FR6.0

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.091 in.)


SR3.0 ZM5SR30 Z26SR30 Z27SR30 Z28SR30



SR4.5 — Z26SR45 Z27SR45 Z28SR45


SL6.0 ZM5SR60 Z26SR60 Z27SR60 Z28SR60

Short Right SR3.0

SR3.5

SR4.0

SR6.0

SR5.0

SR4.5


Z2 Guide CathetersRIGHT CORONARY CURVES





Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.091 in.)


SCR3.5 ZM5SCR35 Z26SCR35 Z27SCR35 Z28SCR35SCR4.0 ZM5SCR40 Z26SCR40 Z27SCR40 Z28SCR40SCR5.0 ZM5SCR50 Z26SCR50 Z27SCR50 Z28SCR50


ECR3.0

ECR3.5

ECR4.5ECR4.0ECR

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.091 in.)


ECR3.5 — Z26ECR35 Z27ECR35 Z28ECR35ECR4.0 ZM5ECR40 Z26ECR40 Z27ECR40 Z28SCR40ECR4.5 — Z26ECR45 Z27ECR45 Z28ECR45

RBU3.5

RBU4.0

NOTO 3DRC

3DRIGHT


Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.091 in.)

without Sideholes without Sideholes without Sideholes without Sideholes

RBU35 — Z26RBU35* — —RBU40 — Z26RBU40* — —NOTO ZM5NOTO Z26NOTO* Z27NOTO* Z28NOTO*3DRC — Z263DRC — —

3DRIGHT ZM53DRIGHT Z263DRIGHT Z273DRIGHT —

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.091 in.)


SAR1.0 ZM5SAR10 Z26SAR10 Z27SAR10 Z28SAR10SAR2.0 ZM5SAR20 Z26SAR20 Z27SAR20 Z28SAR20


Amplatz Right

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.091 in.)


AR1.0 ZM5AR10 Z26AR10 Z27AR10 Z28AR10AR2.0 ZM5AR20 Z26AR20 Z27AR20 Z28AR20

ALR1-2 ZM5AR12 Z26AR12 Z27AR12 Z28AR12

ALR1-2 is a specialty curve for extra backup

AR2.0AR1.0

ALR1-2


Z2 right coronary curves, continued




Multipurpose

MAC(Multi-Aortic)

MP1

MB1

MB2

Hockey Stick II

Hockey Stick III

El Gamal


Hockey Stick I

MAC3.0

MAC3.5

MAC3.75

MAC4.0

MAC4.5

MAC5.0

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.091 in.)


MB1 ZM5MB1 Z26MB1 Z27MB1 Z28MB1MB2 ZM5MB2 Z26MB2 Z27MB2 Z28MB2MP1 ZM5MP1 Z26MP1 Z27MP1† Z28MP1MP2 — Z26MP2 — —

HockeyStickI ZM5HSI Z26HSI Z27HSI Z28HSIHockeyStickII ZM5HSII Z26HSII Z27HSII Z28HSII

HockeyStickRelaxed — Z26RMHSII Z27RMHSII —HockeyStickIII ZM5HSIII Z26HSIII Z27HSIII Z28HSIII

El Gamal ZM5ELGAMAL Z26ELGAMAL Z27ELGAMAL Z28ELGAMAL

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.091 in.)


MAC3.0 ZM5MAC30 Z26MAC30 Z27MAC30 Z28MAC30MAC3.5 ZM5MAC35 Z26MAC35 Z27MAC35 Z28MAC35

MAC3.75 ZM5MAC375 Z26MAC375 Z27MAC375 Z28MAC375MAC4.0 ZM5MAC40 Z26MAC40 Z27MAC40 Z28MAC40MAC4.5 ZM5MAC45 Z26MAC45 Z27MAC45 Z28MAC45MAC5.0 ZM5MAC50 Z26MAC50 Z27MAC50 Z28MAC50

†Sidehole model not available.*Tospecifysideholes,add“SH”totheendoftheproductcode.

Z2 Guide CathetersOTHER CURVES





Bypass Curves LCB

RCBIMA

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.091 in.)


LCB ZM5LCB Z26LCB Z27LCB Z28LCB

LCB (90 cm) — Z26LCBD Z27LCBD Z28LCBD

RCB ZM5RCB Z26RCB Z27RCB Z28RCB

RCB (90 cm) ZM5RCBD Z26RCBD Z27RCBD Z28RCBD

IMA ZM5IMA Z26IMA Z27IMA Z28IMA

IMA (90 cm) ZM5IMAD Z26IMAD Z27IMAD Z28IMAD

Champ Champ0.5

Champ1.5

Champ1.0

Champ2.0

Champ2.5

Champ3.0

Champ3.5

Champ4.0

Curve Style

5 F(i.D. 0.058 in.)

6 F(i.D. 0.070 in.)

7 F(i.D. 0.081 in.)

8 F(i.D. 0.091 in.)


Champ0.5 ZM5CHAMP05 Z26CHAMP05 Z27CHAMP05 Z28CHAMP05








Z2—other curves, continued




LEFT CORONARY CURVES

Curve Style

6 F(i.D. 0.068 in.)

7 Fwith radiopaque Marker Band

(i.D. 0.081 in.) 8 F

(i.D. 0.091 in.) 9 F

(i.D. 0.103 in.)

without Sideholes* without Sideholes* without Sideholes* without Sideholes*

JL3.0 ZM6JL30 ZT7JL30 ZS8JL30 ZM9JL30JL3.5 ZM6JL35 ZT7JL35 ZS8JL35 ZM9JL35JL4.0 ZM6JL40 ZT7JL40 ZS8JL40 ZM9JL40JL4.5 ZM6JL45 ZT7JL45 ZS8JL45 ZM9JL45JL5.0 ZM6JL50 ZT7JL50 ZS8JL50 ZM9JL50JL6.0 ZM6JL60 ZT7JL60 ZS8JL60 ZM9JL60FL3.0 ZM6FL30 ZT7FL30 ZS8FL30 ZM9FL30FL3.5 ZM6FL35 ZT7FL35 ZS8FL35 ZM9FL35FL4.0 ZM6FL40 ZT7FL40 ZS8FL40 ZM9FL40FL4.5 ZM6FL45 ZT7FL45 ZS8FL45 ZM9FL45FL5.0 ZM6FL50 ZT7FL50 ZS8FL50 ZM9FL50FL6.0 ZM6FL60 — ZS8FL60 ZM9FL60

JCL3.0 ZM6JCL30 ZT7JCL30 ZS8JCL30 ZM9JCL30JCL3.5 ZM6JCL35 ZT7JCL35 ZS8JCL35 ZM9JCL35JCL4.0 ZM6JCL40 ZT7JCL40 ZS8JCL40 ZM9JCL40JCL4.5 ZM6JCL45 ZT7JCL45 ZS8JCL45 ZM9JCL45JCL5.0 ZM6JCL50 ZT7JCL50 ZS8JCL50 ZM9JCL50

Curve Style

6 F(i.D. 0.068 in.)


(i.D. 0.081 in.) 8 F

(i.D. 0.091 in.) 9 F

(i.D. 0.103 in.)


SL3.0 ZM6SL30 ZT7SL30 ZS8SL30 ZM9SL30SL3.5 ZM6SL35 ZT7SL35 ZS8SL35 ZM9SL35SL4.0 ZM6SL40 ZT7SL40 ZS8SL40 ZM9SL40SL4.5 ZM6SL45 ZT7SL45 ZS8SL45 ZM9SL45SL5.0 ZM6SL50 ZT7SL50 ZS8SL50 ZM9SL50SL6.0 ZM6SL60 ZT7SL60 — —

Left Standard

Short Left

SL3.0

SL3.5

SL4.0

SL4.5

SL5.0

SL6.0


JL3.0

JL5.0

JL6.0

JL3.5

JL4.5

JCL3.5

JCL4.0

JCL4.5

JCL5.0

JCL3.0

FL6.0

FL5.0

FL4.5

FL4.0

FL3.5

FL3.0

JL4.0

General Characteristics:Supplied sterile.items per box: 1Zuma® Guide Catheters




Short Amplatz Left

SAL.75

SAL1.0

SAL1.5

SAL2.0 SAL3.0

SAL4.0SAL2.5

Curve Style

6 F(i.D. 0.068 in.)


(i.D. 0.081 in.) 8 F

(i.D. 0.091 in.) 9 F

(i.D. 0.103 in.)


SAL.75 ZM6SAL75 ZT7SAL75 ZS8SAL75 ZM9SAL75SAL1.0 ZM6SAL10 ZT7SAL10 ZS8SAL10 ZM9SAL10SAL1.5 ZM6SAL15 ZT7SAL15 ZS8SAL15 ZM9SAL15SAL2.0 ZM6SAL20 ZT7SAL20 ZS8SAL20 ZM9SAL20SAL2.5 ZM6SAL25 ZT7SAL25 ZS8SAL25 ZM9SAL25SAL3.0 ZM6SAL30 ZT7SAL30 ZS8SAL30 ZM9SAL30SAL4.0 ZM6SAL40 ZT7SAL40 ZS8SAL40 ZM9SAL40

Left Backup Support

EBU (Extra Backup)

EBU3.0

EBU3.5

EBU3.75

EBU5.0EBU4.0

EBU4.5

Curve Style

6 F(i.D. 0.068 in.)


(i.D. 0.081 in.) 8 F

(i.D. 0.091 in.) 9 F

(i.D. 0.103 in.)


EBU3.0 ZM6EBU30 ZT7EBU30 ZS8EBU30 ZM9EBU30EBU3.5 ZM6EBU35 ZT7EBU35 ZS8EBU35 ZM9EBU35

EBU3.75 ZM6EBU375 ZT7EBU375 ZS8EBU375 ZM9EBU375EBU4.0 ZM6EBU40 ZT7EBU40 ZS8EBU40 ZM9EBU40EBU4.5 ZM6EBU45 ZT7EBU45 ZS8EBU45 ZM9EBU45EBU5.0 ZM6EBU50 ZT7EBU50 ZS8EBU50 ZM9EBU50


Amplatz Left AL2.0

AL1.0

AL1.5

AL.75

AL2.5

AL3.0

AL4.0

Curve Style

6 F(i.D. 0.068 in.)


(i.D. 0.081 in.) 8 F

(i.D. 0.091 in.) 9 F

(i.D. 0.103 in.)


AL.75 ZM6AL75 ZT7AL75 ZS8AL75 ZM9AL75AL1.0 ZM6AL10 ZT7AL10 ZS8AL10 ZM9AL10AL1.5 ZM6AL15 ZT7AL15 ZS8AL15 ZM9AL15AL2.0 ZM6AL20 ZT7AL20 ZS8AL20 ZM9AL20AL2.5 ZM6AL25 ZT7AL25 ZS8AL25 ZM9AL25AL3.0 ZM6AL30 ZT7AL30 ZS8AL30 ZM9AL30AL4.0 ZM6AL40 ZT7AL40 ZS8AL40 ZM9AL40

Zuma left coronary curves, continued





JR4.0

JR5.0

JR6.0

JR3.5

JR4.5

JCR3.5

JCR4.0

JCR4.5

JCR5.0

FR3.0

FR3.5

FR4.0

FR4.5

FR5.0

FR6.0

Short Right SR3.0

SR3.5

SR4.0

SR6.0

SR5.0

SR4.5

Curve Style

6 F(i.D. 0.068 in.)


(i.D. 0.081 in.) 8 F

(i.D. 0.091 in.) 9 F

(i.D. 0.103 in.)


SR3.0 ZM6SR30 ZT7SR30 ZS8SR30 ZM9SR30



SR4.5 — — ZS8SR45 ZM9SR45


SR6.0 ZM6SR60 ZT7SR60 — —

Curve Style

6 F(i.D. 0.068 in.)


(i.D. 0.081 in.) 8 F

(i.D. 0.091 in.) 9 F

(i.D. 0.103 in.)


JR3.0 ZM6JR30 ZT7JR30 ZS8JR30 ZM9JR30JR3.5 ZM6JR35 ZT7JR35 ZS8JR35 ZM9JR35JR4.0 ZM6JR40 ZT7JR40 ZS8JR40 ZM9JR40JR4.5 ZM6JR45 ZT7JR45 ZS8JR45 ZM9JR45JR5.0 ZM6JR50 ZT7JR50 ZS8JR50 ZM9JR50JR6.0 ZM6JR60 ZT7JR60 ZS8JR60 ZM9JR60FR3.0 ZM6FR30 ZT7FR30 ZS8FR30 ZM9FR30FR3.5 ZM6FR35 ZT7FR35 ZS8FR35 ZM9FR35FR4.0 ZM6FR40 ZT7FR40 ZS8FR40 ZM9FR40FR4.5 ZM6FR45 ZT7FR45 ZS8FR45 ZM9FR45FR5.0 ZM6FR50 ZT7FR50 ZS8FR50 ZM9FR50FR6.0 ZM6FR60 ZT7FR60 ZS8FR60 ZM9FR60

JCR3.5 ZM6JCR35 ZT7JCR35 ZS8JCR35 ZM9JCR35JCR4.0 ZM6JCR40 ZT7JCR40 ZS8JCR40 ZM9JCR40JCR4.5 ZM6JCR45 ZT7JCR45 ZS8JCR45 ZM9JCR45JCR5.0 ZM6JCR50 ZT7JCR50 ZS8JCR50 ZM9JCR50


Zuma Guide Catheters RIGHT CORONARY CURVES






Curve Style

6 F(i.D. 0.068 in.)


(i.D. 0.081 in.) 8 F

(i.D. 0.091 in.) 9 F

(i.D. 0.103 in.)


SCR3.5 ZM6SCR35 ZT7SCR35 ZS8SCR35 ZM9SCR35SCR4.0 ZM6SCR40 ZT7SCR40 ZS8SCR40 ZM9SCR40SCR5.0 ZM6SCR50 ZT7SCR50 ZS8SCR50 ZM9SCR50


Curve Style

6 F(i.D. 0.068 in.)


(i.D. 0.081 in.) 8 F

(i.D. 0.091 in.) 9 F

(i.D. 0.103 in.)

without Sideholes* with Sideholes without Sideholes* without Sideholes*

SAR1.0 ZM6SAR10 ZT7SAR10SH ZS8SAR10 ZM9SAR10SAR2.0 ZM6SAR20 ZT7SAR20SH ZS8SAR20 ZM9SAR20

3DRIGHTNOTORight Backup Support

Curve Style

6 F(i.D. 0.068 in.)


(i.D. 0.081 in.) 8 F

(i.D. 0.091 in.)


NOTO ZM6NOTO ZT7NOTO ZS8NOTO3DRIGHT ZM63DRIGHT — —

Amplatz Right

ALR1-2 is a specialty curve for extra backup

Curve Style

6 F(i.D. 0.068 in.)


(i.D. 0.081 in.) 8 F

(i.D. 0.091 in.) 9 F

(i.D. 0.103 in.)


AR1.0 ZM6AR10 ZT7AR10 ZS8AR10 ZM9AR10AR2.0 ZM6AR20 ZT7AR20 ZS8AR20 ZM9AR20

ALR1-2 ZM6ALR12 ZT7ALR12 ZS8ALR12 ZM9ALR12

AR2.0AR1.0 ALR1-2

Zuma right coronary curves, continued




MAC(Multi-Aortic)

MAC3.0

MAC3.5

MAC3.75

MAC4.0

MAC4.5

MAC5.0

Curve Style

6 F(i.D. 0.068 in.)


(i.D. 0.081 in.) 8 F

(i.D. 0.091 in.) 9 F

(i.D. 0.103 in.)


MAC3.0 ZM6MAC30 ZT7MAC30 ZS8MAC30 ZM9MAC30MAC3.5 ZM6MAC35 ZT7MAC35 ZS8MAC35 ZM9MAC35

MAC3.75 ZM6MAC375 ZT7MAC375 ZS8MAC375 ZM9MAC375MAC4.0 ZM6MAC40 ZT7MAC40 ZS8MAC40 ZM9MAC40MAC4.5 ZM6MAC45 ZT7MAC45 ZS8MAC45 ZM9MAC45MAC5.0 ZM6MAC50 ZT7MAC50 ZS8MAC50 ZM9MAC50

Multipurpose

MP1

MB1

MB2

Hockey Stick II

Hockey Stick III

El Gamal

Hockey Stick I

Curve Style

6 F(i.D. 0.068 in.)


(i.D. 0.081 in.) 8 F

(i.D. 0.091 in.) 9 F

(i.D. 0.103 in.)


MB1 ZM6MB1 ZT7MB1 ZS8MB1 ZM9MB1MB2 ZM6MB2 ZT7MB2 ZS8MB2 ZM9MB2MP1 — ZT7MP1 — —

HockeyStickI ZM6HSI ZT7HSI ZS8HSI ZM9HSIHockeyStickII ZM6HSII ZT7HSII ZS8HSII ZM9HSIIHockeyStickIII ZM6HSIII ZT7HSIII ZS8HSIII ZM9HSIII

El Gamal ZM6ELGAMAL ZT7ELGAMAL ZS8ELGAMAL ZM9ELGAMAL

Zuma Guide Catheters OTHER CURVES





Bypass Curves LCB RCB IMA

Curve Style

6 F(i.D. 0.068 in.)


(i.D. 0.081 in.) 8 F

(i.D. 0.091 in.) 9 F

(i.D. 0.103 in.)


LCB ZM6LCB ZT7LCB ZS8LCB ZM9LCBLCB (90 cm) ZM6LCBD ZT7LCBD ZS8LCBD ZM9LCBD

RCB ZM6RCB ZT7RCB ZS8RCB ZM9RCBRCB (90 cm) ZM6RCBD ZT7RCBD ZS8RCBD ZM9RCBD

IMA ZM6IMA ZT7IMA ZS8IMA ZM9IMAIMA (90 cm) ZM6IMAD ZT7IMAD ZS8IMAD ZM9IMAD

Champ Champ0.5

Champ1.5

Champ1.0

Champ2.0

Champ2.5

Champ3.0

Champ3.5

Champ4.0

Curve Style

6 F(i.D. 0.068 in.)


(i.D. 0.081 in.) 8 F

(i.D. 0.091 in.) 9 F

(i.D. 0.103 in.)


Champ0.5 Z26CHAMP05 ZT7CHAMP05 ZS8CHAMP05 ZM9CHAMP05Champ1.0 Z26CHAMP10 ZT7CHAMP10 ZS8CHAMP10 ZM9CHAMP10Champ1.5 Z26CHAMP15 ZT7CHAMP15 ZS8CHAMP15 ZM9CHAMP15Champ2.0 Z26CHAMP20 ZT7CHAMP20 ZS8CHAMP20 ZM9CHAMP20Champ2.5 Z26CHAMP25 ZT7CHAMP25 ZS8CHAMP25 ZM9CHAMP25Champ3.0 Z26CHAMP30 ZT7CHAMP30 ZS8CHAMP30 —Champ3.5 Z26CHAMP35 ZT7CHAMP35 ZS8CHAMP35 ZM9CHAMP35Champ4.0 Z26CHAMP40 ZT7CHAMP40 ZS8CHAMP40 ZM9CHAMP40


Zuma—other curves, continued

51

Embolic Protection

Export® AP Aspiration Catheter

General Characteristics:Supplied sterile. includes two syringes, one filter and extension line with stopcock.

Product Code Guide/Sheath Compatibilitywire Compatibility

(in.) Length (cm)

EXPORTAP 6 F min guide ID 0.070" 0.014 140

GEZ6200US7B 7 F min guide ID 0.080" 0.014 145

All brand names, product names or trademarks belong to their respective holders. For distribution in the USA only.


The Export AP Aspiration Catheter uses a manual locking syringe to easily remove embolic material from throughout the arterial system.

IMPORTANT INFORMATION:Prior to use, refer to the Instructions for Use supplied with these devices for indications, contraindications, side effects, suggested procedure, warnings and precautions.

CAUTION: Federal (USA) law restricts these devices to sale by or on the order of a licensed healthcare practitioner. See package inserts for full product information.

Please consult your local Medtronic sales representative for more information.

52

C O R O N A R YEmbolic Protection

Export® XT Aspiration Catheter

General Characteristics:Supplied sterile. includes two syringes, two filters and extension line with stopcock.

The Export XT Aspiration Catheter uses a manual locking syringe to easily remove embolic material from throughout the arterial system.

IMPORTANT INFORMATION:Prior to use, refer to the Instructions for Use supplied with these devices for indications, contraindications, side effects, suggested procedure, warnings and precautions.

CAUTION: Federal (USA) law restricts these devices to sale by or on the order of a licensed healthcare practitioner. See package inserts for full product information.

Please consult your local Medtronic sales representative for more information.

Product Code Guide/Sheath Compatibilitywire Compatibility

(in.) Length (cm)

EXPORTXT 6 F min guide ID 0.070" (5 F sheath) 0.014 140

GEZ6200US7B 6 F min guide ID 0.070" (5 F sheath) 0.014 145

Guardwire® Temporary Occlusion and Aspiration System


The GuardWire System utilizes an atraumatic balloon to occlude the vessel and prevent particu-late debris from moving distally. Intervention is performed over an 0.014" wire. The Export® Aspiration Catheter is then used to aspirate the debris during balloon occlu-sion. This simple, elegant solution to distal protection has been clini-cally proven to reduce cumulative MACE events by 42 percent at 30-day follow-up when compared with non-GuardWire procedures.*

Product CodeGuardwire

wire O.D. (in.)Total Length

(cm)Balloon Occlusion

Range (mm)Distal Tip

Length (cm) Profile (in.)GEZ6200US 0.014 200 3.0–6.0 2.5 0.036GEZ6300US 0.014 300 3.0–6.0 2.5 0.036GEZ5200US 0.014 200 2.5–5.0 2.5 0.028GEZ5300US 0.014 300 2.5–5.0 2.5 0.028

* Donald S. Baim, on behalf of the Saphenous vein graft Angioplasty Free of Emboli Randomized (SAFER) trial investigators, Circulation 2002;105:1285-1290



53

Interventional Guidewires

The Zinger line of guidewires is the latest advancement in highly trackable guidewires with excellent torque control.

• Available with Pro/Pel®siliconecoatingorHydro-Track® hydrophilic coating for more treatment strategies.

• Zinger is available in various support levels as well as a marker version to meet your preference and clinical challenge.

• 2-cm radiopaque tip for visibility.

Product Product Code Tip Configuration Length (cm) Coating Comments

ZINGER LS ZNGRLS180HS Straight tip 180 Hydro-Track DOC CompatibleZINGER LS ZNGRLS180S Straight tip 180 Pro/Pel DOC CompatibleZINGER LS ZNGRLS180HJ J-tip 180 Hydro-Track DOC CompatibleZINGER LS ZNGRLS180J J-tip 180 Pro/Pel DOC CompatibleZINGER LS ZNGRLS300HS Straight tip 300 Hydro-TrackZINGER LS ZNGRLS300S Straight tip 300 Pro/PelZINGER LS ZNGRLS300HJ J-tip 300 Hydro-TrackZINGER LS ZNGRLS300J J-tip 300 Pro/Pel


ZINGER MK ZNGRMK180HS Straight tip 180 Hydro-Track DOC CompatibleZINGER MK ZNGRMK180S Straight tip 180 Pro/Pel DOC CompatibleZINGER MK ZNGRMK180HJ J-tip 180 Hydro-Track DOC CompatibleZINGER MK ZNGRMK180J J-tip 180 Pro/Pel DOC CompatibleZINGER MK ZNGRMK300HS Straight tip 300 Hydro-TrackZINGER MK ZNGRMK300S Straight tip 300 Pro/PelZINGER MK ZNGRMK300HJ J-tip 300 Hydro-TrackZINGER MK ZNGRMK300J J-tip 300 Pro/Pel

Zinger Light

Zinger Marker

1 cm 1 cm 2 cmMeasuring zoneTip style: Forming ribbonOuter coating:Hydro-Track or Pro/PelTip Stiffness Support

Tip style: Forming ribbonOuter coating:Hydro-Track or Pro/PelTip Stiffness Support

Zinger® Stainless Steel workhorse Guidewire (0.014-in.)

Important InformationPrior to use, refer to the Instructions for Use supplied with these devices for indications, contraindications, side effects, suggested procedure, warnings and precautions.Indications for UseMedtronic guide wires are steerable guide wires that are used for the introduc-tion and placement of diagnostic or interventional devices in the coronary and peripheral vasculature and may be used to reach and cross a target lesion. Medtronic guide wires are not intended for use in cerebral vasculature. Medtronic steerable exchange guide wires are used to facilitate the substitution of one diagnostic or interventional device for another.

Potential Adverse Events:The following complications may be associated with the use of guide wire devices; excessive bleeding, air embolism, ischemia, hematoma at the puncture site, infection, vessel spasm, vascular thrombosis and vessel dissection and perforation.CAUTIONFederal (USA) law restricts these devices to sale by or on the order of a licensed healthcare practitioner. See package inserts for full product information. Please contact your local Medtronic sales representative for more information.Test data on file at Medtronic, Inc. Bench test results may not be indicative of clinical performance.

Zinger guidewires are continued on the next page


© 2011 Medtronic, Inc. All rights reserved. UC200104301gEN 6/11


54




C O R O N A R YInterventional Guidewires


ZINGER S ZNGRS190HS Straight tip 180 Hydro-Track DOC CompatibleZINGER S ZNGRS190S Straight tip 180 Pro/Pel DOC CompatibleZINGER S ZNGRS190HJ J-tip 180 Hydro-Track DOC CompatibleZINGER S ZNGRS190J J-tip 180 Pro/Pel DOC CompatibleZINGER S ZNGRS300HS Straight tip 300 Hydro-TrackZINGER S ZNGRS300S Straight tip 300 Pro/PelZINGER S ZNGRS300HJ J-tip 300 Hydro-TrackZINGER S ZNGRS300J J-tip 300 Pro/Pel

Zinger Support


Zinger, continued


ZINGER MS ZNGRMS180HS Straight tip 180 Hydro-Track DOC CompatibleZINGER MS ZNGRMS180S Straight tip 180 Pro/Pel DOC CompatibleZINGER MS ZNGRMS180HJ J-tip 180 Hydro-Track DOC CompatibleZINGER MS ZNGRMS180J J-tip 180 Pro/Pel DOC CompatibleZINGER MS ZNGRMS300HS Straight tip 300 Hydro-TrackZINGER MS ZNGRMS300S Straight tip 300 Pro/PelZINGER MS ZNGRMS300HJ J-tip 300 Hydro-TrackZINGER MS ZNGRMS300J J-tip 300 Pro/Pel

Zinger Medium


55






Intuition INTU180S Straight tip 180 Hydro-Track DOC CompatibleIntuition INTU180SS Straight tip 180 Pro/Pel DOC CompatibleIntuition INTU300S Straight tip 300 Hydro-TrackIntuition INTU300SS Straight tip 300 Pro/Pel

Tip style: Core-to-tipOuter coating:Hydro-Track or Pro/PelTip Stiffness Support

Intuition 3 cm

The Intuition Guidewire offers torque performance and one-gram tip weight to give precision and confidence during more difficult workhorse cases. • Rounded tip and body provide control.• Accu-Core technology provides torque performance to

control and direct the wire.

• Femoral (proximal) markers on wire, 90 cm and 100 cm from distal tip.

• Available with Pro/Pel®siliconecoatingorHydro-Track® hydrophilic coating for more treatment strategies.


Intuition Stainless Steel Advanced workhorse Guidewire (0.014-in.)

56







The Cougar Steerable Guidewire offers the performance and support required for workhorse cases.

• Nitinol core wire.

• Double coil tip design offers a soft tip with outstanding tip shape retention.

• AvailableinHydro-Track® hydrophilic or Pro/Pel® silicone coating.

– TheHydro-Trackhydrophiliccoatingoffersoptimallubricity and durability.

– The Pro/Pel silicone coating offers traditional performance for situations that require reduced lubricity.



COUGAR LS CGRLS190HS Straight tip 190 Hydro-Track DOC CompatibleCOUGAR LS CGRLS190S Straight tip 190 Pro/Pel DOC CompatibleCOUGAR LS CGRLS190HJ J-tip 190 Hydro-Track DOC CompatibleCOUGAR LS CGRLS190J J-tip 190 Pro/Pel DOC CompatibleCOUGAR LS CGRLS300HS Straight tip 300 Hydro-TrackCOUGAR LS CGRLS300S Straight tip 300 Pro/PelCOUGAR LS CGRLS300HJ J-tip 300 Hydro-TrackCOUGAR LS CGRLS300J J-tip 300 Pro/Pel


COUGAR XT CGRXT190HS Straight tip 190 Hydro-Track DOC CompatibleCOUGAR XT CGRXT190S Straight tip 190 Pro/Pel DOC CompatibleCOUGAR XT CGRXT190HJ J-tip 190 Hydro-Track DOC CompatibleCOUGAR XT CGRLS190J J-tip 190 Pro/Pel DOC CompatibleCOUGAR XT CGRXT300HS Straight tip 300 Hydro-TrackCOUGAR XT CGRXT300S Straight tip 300 Pro/PelCOUGAR XT CGRXT300HJ J-tip 300 Hydro-TrackCOUGAR XT CGRXT300J J-tip 300 Pro/Pel

Cougar LS— Light Support

Cougar XT— Medium Support

3 cm

Cougar® Nitinol workhorse Guidewire (0.014-in.)

57





The Thunder Guidewire has a stainless steel core-to-tip design that provides enhanced support and stability while maintaining excellent torque characteristics with precise tip control and steering.

• Short transition zone (rail) provides support for accurate device placement.

• Pro/Pel® silicone coating.

• 3 cm radiopaque tip for visibility.

Thunder® Stainless Steel Extra-Support Guidewire (0.014-in.)


THUNDER THNDR190S Straight tip 190 Pro/Pel DOC CompatibleTHUNDER THNDR190J J Tip 190 Pro/Pel DOC CompatibleTHUNDER THNDR300S Straight tip 300 Pro/PelTHUNDER THNDR300J J Tip 300 Pro/Pel

Tip style: Core-to-tipOuter coating: Pro/PelTip Stiffness Support

3 cm

58





ProVia 3

ProVia 6

ProVia 9

ProVia 12





3 cm

Product Product Code Size (g) Tip Configuration Length (cm) Coating CommentsProVia 3 3PROV180HS 3 Straight tip 180 Hydro-Track DOC CompatibleProVia 3 3PROV180SS 3 Straight tip 180 Pro/Pel DOC CompatibleProVia 3 3PROV300HS 3 Straight tip 300 Hydro-TrackProVia 3 3PROV300SS 3 Straight tip 300 Pro/Pel

Product Product Code Size (g) Tip Configuration Length (cm) Coating CommentsProVia 6 6PROV180HS 6 Straight tip 180 Hydro-Track DOC CompatibleProVia 6 6PROV180SS 6 Straight tip 180 Pro/Pel DOC CompatibleProVia 6 6PROV300HS 6 Straight tip 300 Hydro-TrackProVia 6 6PROV300SS 6 Straight tip 300 Pro/Pel

Product Product Code Size (g) Tip Configuration Length (cm) Coating CommentsProVia 9 9PROV180HS 9 Tapered tip 180 Hydro-Track DOC CompatibleProVia 9 9PROV180SS 9 Tapered tip 180 Pro/Pel DOC CompatibleProVia 9 9PROV300HS 9 Tapered tip 300 Hydro-TrackProVia 9 9PROV300SS 9 Tapered tip 300 Pro/Pel

Product Product Code Size (g) Tip Configuration Length (cm) Coating CommentsProVia 12 12PROV180HS 12 Tapered tip 180 Hydro-Track DOC CompatibleProVia 12 12PROV180SS 12 Tapered tip 180 Pro/Pel DOC CompatibleProVia 12 12PROV300HS 12 Tapered tip 300 Hydro-TrackProVia 12 12PROV300SS 12 Tapered tip 300 Pro/Pel

The ProVia Crossing Guidewire is designed to cross demanding lesions. • Accu-Core wire technology is designed to provide torque performance to

control and direct the wire. • Rounded tip and body provide control.• Tapered tip on ProVia 9 and 12 wires.• 1-mm noncoated tip on the hydrophilic version.

• Femoral (proximal) markers on wire, 90 cm and 100 cm from distal tip.• AvailableinHydro-Track® hydrophilic or Pro/Pel® silicone coating.

– TheHydro-Trackhydrophiliccoatingoffersoptimallubricityanddurability. – The Pro/Pel silicone coating offers traditional performance for situations that require reduced lubricity.


ProVia Stainless Steel Crossing Guidewire (0.014-in.)

Straight tip (0.014 in.)

Straight tip (0.014 in.)

Tapered tip (0.009 in.)

Tapered tip (0.009 in.)

59

The unique coronary catheter shaft design incorporates a wire braid for responsive torque control and columnar strength. The polymer inner and outer jackets provide a large inner lumen for easy hand injection and clear images.

The ergonomic hub allows for comfortable catheter manipulations and includes a color-coded luer for easy size identification.

The soft tip allows for gentle ostial intubation.SiteSeer catheters are engineered to withstand an injection pressure of: 1195 psi: 6 F pigtail catheters 1200 psi: All coronary and 5 F pigtail catheters

5 FCoronary and

pigtail catheters

6 FCoronary catheters

i.D. = 0.045" i.D. = 0.055"

6 FPigtail catheters

i.D. = 0.050"

Pebax innerjacket

Double-braided shaft

Pebax outerjacket

Strainrelief

ergonomic hub Color-codedluer

Inner Diameters

4 FCoronary and

pigtail catheters

i.D. = 0.042"

DIAGNOSTICS AND ACCESSORIES

Angiographic Catheters

SiteSeer® Angiographic Catheters

Catheter Construction 5/6 F SiteSeer Catheters

All curve styles have an atraumatic soft tip, with the exception of the pigtail curves. “XT” shafts on 6 F pigtails provide extra support for valve crossability.

Product Code French Size Items per Box Sideholes Length (cm)

4A0025 4 10 6 1254A0028 4 10 6 1105A0028 5 10 6 1106A0092 6 (XT) 10 6 110

Straight Tight Radius Pigtail


5A0069 5 10 6 1105A0094 5 10 6 1256A0031 6 10 6 1106A0079 6 10 6 1256A0028 6 10 12 1106A0077 6 (XT) 10 6 1106A0069 6 (XT) 10 12 1106A0027 6 (XT) 10 6 125

Straight Pigtail

General Characteristics:Supplied sterile.Color-coded luer and packaging.Maximum guidewire: 4 F = 0.035"

5/6 F = 0.038"


© 2011 Medtronic, Inc. All rights reserved. UC200104302eEN 11/11

60

C O R O N A R YDiagnostics and Accessories—




155°


5A0071 5 10 6 1106A0030 6 10 12 1106A0071 6 (XT) 10 12 110

Van Tassel 155° Angled Pigtail


Product Code French Size Items per Box Length (cm)

5A0084 5 5 1006A0080 6 5 100

Judkins Left 3.5


4A0010 4 5 1005A0010 5 5 1006A0010 6 5 100

Judkins Left 3.5 I

145°


4A0026 4 10 6 1254A0029 4 10 6 1105A0029 5 10 6 1106A0093 6 (XT) 10 6 110

145° Angled Tight Radius Pigtail

155°


4A0027 4 10 6 1254A0030 4 10 6 1105A0030 5 10 6 110

155° Angled Tight Radius Pigtail

145°


5A0070 5 10 6 1106A0032 6 10 6 1106A0029 6 10 12 1106A0078 6 (XT) 10 6 1106A0070 6 (XT) 10 12 110

Van Tassel 145° Angled Pigtail

General Characteristics:Supplied sterile.Color-coded luer and packaging.Maximum guidewire: 4 F = 0.035" 5/6 F = 0.038"

SiteSeer® Angiographic Catheters, continued

61






5A0086 5 5 1006A0082 6 5 100

Judkins Left 4.5

Product Code French Size items per Box Length (cm)

4A0068 4 5 1005A0060 5 5 1006A0012 6 5 100

Judkins Left 4.5 I



5A0085 5 10 1005A0089 5 10 1256A0085 6 10 100

6A0087 6 10 125

Judkins Left 4.0


4A0011 4 10 1004A0040 4 10 1255A0011 5 10 1005A0040 5 10 1256A0011 6 10 1006A0042 6 10 125

Judkins Left 4.0 I


5A0087 5 5 1006A0083 6 5 100

Judkins Left 5.0


4A0012 4 5 1005A0012 5 5 1006A0013 6 5 100

Judkins Left 5.0 I

Judkins Left 6.0 I Product Code French Size Items per Box Length (cm)

4A0013 4 5 1005A0013 5 5 1006A0014 6 5 100



62






4A0007 4 5 1005A0007 5 5 1006A0007 6 5 100

3D Right Coronary


4A0006 4 5 1005A0006 5 5 1006A0006 6 5 100

No Torque Right


4A0001 4 5 1005A0001 5 5 1006A0001 6 5 100

Judkins Right 3.5

Judkins Right 4.0 Product Code French Size Items per Box Length (cm)

5A0002 5 10 1005A0088 5 10 1256A0002 6 10 1006A0086 6 10 125

Judkins Right 4.0 I Product Code French Size Items per Box Length (cm)

4A0002 4 10 1004A0041 4 10 1255A0075 5 10 1005A0041 5 10 1256A0075 6 10 1006A0043 6 10 125


4A0003 4 10 1005A0003 5 10 1006A0003 6 10 100

Modified Judkins Right 4.0


4A0004 4 5 1005A0004 5 5 1006A0004 6 5 100

Judkins Right 5.0




63






4A0005 4 5 1005A0005 5 5 1006A0005 6 5 100

Judkins Right 6.0


4A0018 4 5 1005A0018 5 5 1006A0020 6 5 100

Amplatz Left I


4A0019 4 5 1005A0019 5 5 1006A0021 6 5 100

Amplatz Left II



4A0020 4 5 1005A0020 5 5 1006A0022 6 5 100

Amplatz Left III

Amplatz Right I Product Code French Size Items per Box Length (cm)

4A0016 4 5 1005A0016 5 5 1006A0018 6 5 100

Modified Amplatz Right Product Code French Size Items per Box Length (cm)

4A0067 4 5 1005A0068 5 5 1006A0017 6 5 100


4A0017 4 5 1005A0017 5 5 1006A0019 6 5 100

Amplatz Right II



64





Champ 1.0 Product Code French Size Items per Box Length (cm)

4A0009 4 5 1005A0009 5 5 1005A0045 5 5 1106A0009 6 5 1006A0047 6 5 110


4A0008 4 5 1004A0044 4 5 1105A0008 5 5 1005A0044 5 5 1106A0008 6 5 1006A0046 6 5 110


5A0014 5 5 1005A0046 5 5 1106A0015 6 5 1006A0048 6 5 110


5A0015 5 5 1005A0047 5 5 1106A0016 6 5 1006A0049 6 5 110

Multipurpose A-1 Product Code French Size Items per Box Length (cm)

4A0021 4 5 1004A0048 4 5 1105A0021 5 5 1005A0048 5 5 1106A0023 6 5 1006A0050 6 5 110

Multipurpose A-2 (two sideholes)


4A0022 4 5 1004A0049 4 5 1105A0022 5 5 1005A0049 5 5 1106A0024 6 5 1006A0051 6 5 110




65





Left Coronary Bypass Product Code French Size Items per Box Length (cm)

4A0032 4 5 1005A0032 5 5 1006A0034 6 5 100

Multipurpose B-2 (two sideholes)


4A0024 4 5 1004A0051 4 5 1105A0024 5 5 1005A0051 5 5 1106A0026 6 5 1006A0053 6 5 110

Multipurpose B-1 Product Code French Size Items per Box Length (cm)

4A0023 4 5 1004A0050 4 5 1105A0023 5 5 1005A0050 5 5 1106A0025 6 5 1006A0052 6 5 110

Right Coronary Bypass Product Code French Size Items per Box Length (cm)

4A0033 4 5 1005A0033 5 5 1006A0035 6 5 100

Internal Mammary Artery Product Code French Size Items per Box Length (cm)

4A0031 4 5 1005A0031 5 5 1006A0033 6 5 100


Sones® A (two sideholes)


4A0037 4 5 1005A0055 5 5 805A0037 5 5 1006A0057 6 5 806A0039 6 5 100

Sones B (two sideholes)


5A0056 5 5 805A0038 5 5 1006A0058 6 5 806A0040 6 5 100



66





Sones C (two sideholes)


5A0039 5 5 1006A0059 6 5 806A0041 6 5 100

Brachial 3.5 (one sidehole)


4A0034 4 5 1005A0052 5 5 805A0034 5 5 1006A0054 6 5 806A0036 6 5 100



4A0035 4 5 1005A0053 5 5 805A0035 5 5 1006A0055 6 5 806A0037 6 5 100



5A0054 5 5 805A0036 5 5 1006A0056 6 5 806A0038 6 5 100

El Gamal I

Arani l

Arani ll

Alternative Product Code Description French Size Items per Box Length (cm)

4A0042 Arani I 4 5 100

5A0042 Arani I 5 5 100

6A0044 Arani I 6 5 100

6A0045 Arani II 6 5 100

5A0059 El Gamal I 5 5 100

6A0061 El Gamal I 6 5 100



SiteSeer® Angiographic Catheters

67





Packaging Options for SiteSeer® CathetersAngio-Kits

Angio-Kit contains:

• One Judkins Right 4-cm catheter (JR4.0)

• One Judkins Left I 4-cm catheter (JL4.0 I)

• One straight or angled pigtail catheter:

Straight Pigtail Catheter

145°

145° Angled Pigtail Catheter

155°


Judkins right 4-cm catheter

Judkins Left i 4-cm catheter

Product Code French Size Pigtail Curve Pigtail Sideholes

4A0061 4 Straight 65A0062 5 Straight 66A0063 6 Straight 126A0102 6 XT straight 6


4A0062 4 145° angle 65A0063 5 145° angle 66A0064 6 145° angle 126A0103 6 XT 145° angle 6


4A0063 4 155° angle 65A0064 5 155° angle 66A0065 6 155° angle 12


145°


Judkins Left i 4-cm Catheter

Angio-Kit contains:

• One 3-D Right catheter



3-D right Catheter


4A0069 4 Straight 65A0072 5 Straight 66A0072 6 XT straight 6


5A0095 5 145° angle 66A0108 6 XT 145° angle 6

General Characteristics:Supplied sterile.Angio-Kits per box: 5Maximum guidewire: see label“Xt” shafts on 6 F pigtails provide extra support for valve crossability

68





Angiography kit contains:

• One 0.035" 3-mm “J” 145-cm length standard taper guidewire



• One Input® PS introducer sheath



• One 0.035" 3-mm “J” 145-cm-length standard taper guidewire

• One 3-D Right catheter


• One Input PS introducer sheath

• One straight pigtail catheter:

0.035" 3-mm “J” Standard taper Guidewire

0.035” 3-mm “J” Standard taper Guidewire



145°


155°


input PS introducer Sheath


Judkins right 4-cm Catheter

Packaging Options for SiteSeer CathetersEZ-Pak® Angiography Kits—0.035" Guidewire




5A0066 5 145° angle 66A0067 6 145° angle 126A0106 6 XT 145° angle 6


5A0067 5 155° angle 66A0068 6 155° angle 12

3-D Right Catheter


5A0073 5 Straight 66A0073 6 XT straight 6



General Characteristics:Supplied sterile.Angio-Kits per box: 5“Xt” shafts on 6 F pigtails provide extra support for valve crossability

69











0.038" 3-mm “J” Standard taper Guidewire

Packaging Options for SiteSeer® CathetersEZ-Pak® Angiography Kit—0.038" Guidewire




5A0093 5 145° angle 66A0101 6 145° angle 126A0107 6 XT 145° angle 6


Judkins right 4-cm Catheter



145°


General Characteristics:Supplied sterile.Angio-Kits per box: 5“Xt” shafts on 6 F pigtails provide extra support for valve crossability

70





Pro-Flo® Angiographic CathetersPro-FloStandard•Pro-FloSoftTip•Pro-FloXT•Pro-FloXTSoftTip

The Pro-Flo® catheter was designed with a high-strength polyurethane. The wire braid assures a 1:1 torque response.

Internal Diameters

6 F Pro-Flo 7 F Pro-Flo

i.D. = 0.050" i.D. = 0.061"

Winged Hub

Polyurethane Overjacket

Wire Overbraid

Catheter Construction—Pro-Flo Standard and Pro-Flo with Soft Tip

Color- Coded Strain relief

High-Strength Polyurethane inner Core

145°145° Angled Pigtail


145°

Straight tight radius Pigtail

145° Angled tight radius Pigtail

Product Code French Size Tip Curve Style Sideholes Length (cm)006803 6 Straight 6 110006465 6 Straight 12 110010245 7 Straight 6 110010306 7 Straight 12 110

Product Code French Size Tip Curve Style Sideholes Length (cm)060016 6 Straight TR 12 110060018 6 145° angled TR 12 110

Product Code French Size Tip Curve Style Sideholes Length (cm)006804 6 145° angled 6 110006896 6 145° angled 12 110006897 6 155° angled 12 110010246 7 145° angled 6 110010307 7 145° angled 12 110010308 7 155° angled 12 110

Straight Pigtail

Van Tassel Angled Pigtail

Tight Radius Pigtail

Pro-Flo Standard

General Characteristics:Supplied sterile.Color-coded strain relief and packaging.Maximum guidewire: 0.038"items per box: 10

71





Judkins Right Coronary Product Code French Size Tip Curve Length (cm) Length (cm)006454 6 3.5 100006455 6 4.0 100006456 6 5.0 100010303 7 3.5 100010304 7 4.0 100010305 7 5.0 100

Judkins Left Coronary Product Code French Size Tip Curve Length (cm) Length (cm)006451 6 3.5 100006452 6 4.0 100060034 6 4.5 100006453 6 5.0 100010300 7 3.5 100010301 7 4.0 100010302 7 5.0 100

Left lll

Left ll

Left l

Right ll

Right l

Amplatz Product Code French Size Tip Curve Style Length (cm)006457 6 Right I 100006458 6 Right II 100006459 6 Left I 100006460 6 Left II 100060039 6 Left III 100010309 7 Right I 100010310 7 Right II 100010311 7 Left I 100010312 7 Left II 100

Left i

right i

Coronary Bypass Product Code French Size Tip Curve Style Length (cm)

006461 6 Left I 100006462 6 Right I 100010313 7 Left I 100010314 7 Right I 100

iMA

Internal Mammary Artery Product Code French Size Tip Curve Style Length (cm)

006470 6 IMA 100010315 7 IMA 100

Multipurpose Product Code French Size Tip Curve Style Length (cm)

006463 6 A-1 100006464 6 A-2 100010316 7 A-1 100010317 7 A-2 110

A-1A-2


Pro-Flo® Standard Angiographic Catheters, continued

72





Pro-Flo® Soft Tip Angiographic Catheters

Catheter Construction — Pro-Flo Soft TipAtraumatic tapered tip Soft tip

Segment

Product Code French Size Tip Curve Length (cm) Length (cm)

010014 6 3.5 100010015 6 4.0 100060032 6 4.5 100010016 6 5.0 100010164 6 6.0 100004910 7 3.5 100004911 7 4.0 100060050* 7 4.0* 100060035 7 4.5 100004912 7 5.0 100004945 7 6.0 100

* Short Tip.

Product Code French Size Tip Curve Length (cm) Length (cm)

010017 6 3.5 100010018 6 4.0 100010019 6 5.0 100010165 6 6.0 100004913 7 3.5 100004914 7 4.0 100004915 7 5.0 100004946 7 6.0 100

Judkins Left Coronary

Judkins Right Coronary


Internal Diameters


i.D. = 0.050" i.D. = 0.061"

• Atraumatic tip, gradually tapering to 5.5 F.

• The Pro-Flo Soft Tip catheter features a soft tip designed to help reduce the risk of artery dissection and vessel trauma.

• With their unique configuration, Pro-Flo XT catheters provide a stiffer shaft.

73





A-1

A-2

B-1

B-2

Product Code French Size Tip Curve Style Length (cm)

010032 6 A-1 100060047 6 A-1 125010024 6 A-2 100060042 6 A-2 125010215 6 B-1 100010216 6 B-2 100004923 7 A-1 100060044 7 A-2 125004947 7 B-1 100004948 7 B-2 100

Multipurpose

no torque right Coronary Catheter

No Torque Right coronary catheters allow you to engage the RCA without manipulation.




010026 6 IMA 100004922 7 IMA 100


009228 6 No Torque Right 100009229 7 No Torque Right 100

Internal Mammary Artery

No Torque Right Coronary

Left i

iMA

right i

Coronary Bypass


010020 6 Right I 100010021 6 Right II 100004951 6 Modified Right 100010022 6 Left I 100010023 6 Left II 100060046 6 Left III 100004916 7 Right I 100004917 7 Right II 100009230 7 Modified Right 100004925 7 Left I 100004919 7 Left II 100060040 7 Left III 100

Amplatz

Left lll

Left ll

Left l

Right ll

Right l

Soft tip

Pro-Flo® Soft tip Angiographic Catheters, continued

74





Pro-Flo® XT Angiographic Catheter

Product Code French Size Tip Curve Style Sideholes Length (cm)

010241 6 Straight 6 110060048 6 Straight 6 125010340 6 Straight 12 110010243 7 Straight 6 110010355 7 Straight 12 110


010242 6 145° angled 6 110010341 6 145° angled 12 110060049 6 145° angled 6 125010342 6 155° angled 12 110010244 7 145° angled 6 110010356 7 145° angled 12 110010357 7 155° angled 12 110


060017 6 Straight TR 12 110060019 6 145° angled TR 12 110

Straight Pigtail

Tight Radius Pigtail



145°

Straight tight radius Pigtail

145° Angled tight radius Pigtail

A-2


010321 6 A-2 110010358 7 A-2 110

Multipurpose


• Atraumatic tip, gradually tapering to 5.5 F.

• The Pro-Flo® Soft Tip catheter features a soft tip designed to help reduce the risk of artery dissection and vessel trauma.

• With their unique configuration, Pro-Flo XT catheters provide a stiffer shaft.

Internal Diameters


i.D. = 0.050" i.D. = 0.061"

Van Tassel Angled Pigtail

75





Pro-Flo® XT Soft Tip Angiographic Catheter

Judkins Left Coronary

Judkins Right Coronary

Product Code French Size Tip Curve Length (cm) Length (cm)010345 6 3.5 100010343 6 4.0 100060051 6 4.0 125060033 6 4.5 100010344 6 5.0 100010160 6 6.0 100010359 7 3.5 100010360 7 4.0 100060036 7 4.5 100010361 7 5.0 100010162 7 6.0 100

Product Code French Size Tip Curve Length (cm) Length (cm)010319 6 3.5 100010318 6 4.0 100060052 6 4.0 125010320 6 5.0 100010161 6 6.0 100010362 7 3.5 100010363 7 4.0 100010364 7 5.0 100010163 7 6.0 100

Left lll

Left ll

Left l

Right ll

Right l

Product Code French Size Tip Curve Style Length (cm)010346 6 Right I 100010347 6 Right II 100009231 6 Modified Right 100010348 6 Left I 100010349 6 Left II 100060038 6 Left III 100010365 7 Right I 100010366 7 Right II 100010052 7 Modified Right 100010367 7 Left I 100010368 7 Left II 100

Amplatz


Catheter Construction — Pro-Flo Soft TipAtraumatic tapered tip

Soft tip Segment

Internal Diameters


i.D. = 0.050" i.D. = 0.061"

The unique XT polymer overjacket is resistant to softening at body temperature, an important benefit in extended cases.

The Pro-Flo XT has the same internal diameter and high flow rates as the standard Pro-Flo catheters.

The Pro-Flo XT catheter features a soft tip designed to help reduce the risk of artery dissection and vessel trauma.

Atraumatic tip, gradually tapering to 5.5 F.

76






010353 6 A-1 100010354 6 A-2 110010212 6 B-1 100010213 6 B-2 100010372 7 A-1 100010373 7 A-2 110010247 7 B-1 100010248 7 B-2 100

Multipurpose




009234 6 No Torque Right 100009235 7 No Torque Right 100


010352 6 IMA 100010371 7 IMA 100

A-1

A-2

B-1

B-2

no torque right Coronary Catheter

Product Description: No Torque Right coronary catheters allow you to engage the RCA without manipulation.

Internal Mammary Artery

No Torque Right Coronary

Left i

iMA

right i

Coronary Bypass

Pro-Flo® Xt Soft tip Angiographic Catheters, continued

77





Packaging Options for Pro-Flo® Angiographic CathetersAngio-Kits

Product Code French Size Design Style

008419 6 Pro-Flo008420 6 Pro-Flo with soft tip018418 6 Pro-Flo XT with soft tip004901 7 Pro-Flo004902 7 Pro-Flo with soft tip014903 7 Pro-Flo XT with soft tip


038443 6 Pro-Flo with soft tip038445 6 Pro-Flo XT with soft tip038450 7 Pro-Flo with soft tip038451 7 Pro-Flo XT with soft tip


038448 6 Pro-Flo XT with soft tip

Angio-Kit contains:


• One Judkins Left 4-cm catheter (JL4.0)


Straight Pigtail catheter

145°

145° Angled Pigtail catheter

155°



Judkins Left i 4-cm catheter

General Characteristics:Supplied sterile.Maximum guidewire: 0.038"Angio-Kits per box: 5

78





Packaging Options for Pro-Flo® Angiographic CathetersEZ-Pak® Angiography Kits—0.035" Guidewire


558447 6 Pro-Flo with soft tip558448 6 Pro-Flo XT with soft tip558453 7 Pro-Flo with soft tip

EZ-Pak® Angiography Kit contains:






0.035" 3-mm “J” standard taper guidewire


145°


155°


input PS introducer sheath


Judkins Left 4-cm catheter




558420 6 Pro-Flo with soft tip558418 6 Pro-Flo XT with soft tip554903 7 Pro-Flo XT with soft tip

General Characteristics:Supplied sterile.Maximum guidewire: 0.038"Angio-Kits per box: 5

79






Packaging Options for Pro-Flo® Angiographic CathetersEZ-Pak® Angiography Kits—0.038" Guidewire




858443 6 Pro-Flo with soft tip858445 6 Pro-Flo XT with soft tip


858448 6 Pro-Flo XT with soft tip

EZ-Pak® Angiography Kit contains:

• One 0.038" 3-mm “J” 145-cm length standard taper guidewire





0.038" 3-mm “J” standard taper guidewire


145°


155°



Judkins Left 4-cm catheter

General Characteristics:Supplied sterile.Angio-Kits per box: 5

80





The Sones coronary catheter was developed with F. Mason Sones, MD, to meet the evolving clinical needs of the brachial angiographer.

Two unique design features:

• The woven core provides torque control.

• The tapered tip adapts to anatomical variations.

Medtronic supplies a variety of catheter constructions and curve style tips as illustrated.

Sones® woven Coronary Catheters

Typical Sones Catheter Tip

8 F shaft 1.5 in.tip length

5.5 F tip1 in.taper length

Construction Styles

7 F Standard

Sones Hi-Flow

8 F Standard Nylon Core

Sones Positrol® Nylon Core

Polyurethane buildup Woven core

Polyurethane buildup Woven outer core

Wire braid

nylon inner core (thin wall)


Wire braid nylon inner core


nylon inner core

Sones Positrol woven Core

Polyurethane buildup Wire braid Woven inner core

General Characteristics:Supplied sterile.Maximum guidewire:

7 F, 7.5 F and 8 F standard: 0.035"7 F and 8 F Hi-Flow: 0.038"

items per box: 10

81






Product Code French Size Length (cm) Tip Length (in.) Minimum Tip I.D. (in.) Comments

007764 7 80 1.5 0.036 Extra stiffness—tip & shaft007536 7 100 1.5 0.036


008976 7 80 1.5 0.040008977 7 100 1.5 0.040008718 8 80 1.5 0.040008971 8 100 1.5 0.040


007538 8 80 1.5 0.036007539 8 100 1.5 0.036007766 8 80 1.5 0.036 Extra stiffness—tip & shaft007540 8 125 1.5 0.036


008541 7.5 100 1.5 0.036 Extra stiffness—shaft

Standard

Hi-Flow

Standard Nylon Core

Positrol® Nylon Core

Curve Style A

1.0" (2.54 cm) curve length for normal aortic roots


007548 7 100 1.5 0.036


008978 7 80 1.5 0.040008979 7 100 1.5 0.040008719 8 80 1.5 0.040


007550 8 80 1.5 0.036007551 8 100 1.5 0.036


008554 7.5 100 1.5 0.036 Extra stiffness—shaft


007561 7.5 80 1.5 0.036 Wire-reinforced007562 7.5 100 1.5 0.036 Wire-reinforced

Standard

Hi-Flow

Standard Nylon Core

Positrol Nylon Core

Positrol woven Core

Curve Style B

General Characteristics:Supplied sterile.Maximum guidewire:

7 F, 7.5 F and 8 F standard: 0.035"7 F and 8 F Hi-Flow: 0.038"

items per box: 10

All tips taper to 5.5 F.


82







008980 7 80 1.5 0.040008981 7 100 1.5 0.040008720 8 80 1.5 0.040


008538 7.5 80 1.5 0.036008539 7.5 100 1.5 0.036008356 8 80 1.5 0.036 Standard nylon core


007770 8 80 Long tip 0.036007771 8 100 Long tip 0.036


008358 8 80 1.5 0.036 Straight tip008359 8 100 1.5 0.036 Straight tip

Curve Style C

Positrol® Nylon Core

Brachial LTX-S

Standard Nylon Core

Hi-Flow

General Characteristics:Supplied sterile.Maximum guidewire: 7 F, 7.5 F and 8 F standard: 0.035" 7 F and 8 F Hi-Flow: 0.038"items per box: 10


83





woven Coronary Catheters—High-Volume

Pediatric product.

There are four high-volume angiographic catheters designed to facilitate large-volume contrast studies. The construction style consists of a woven outer core and a polyurethane buildup with a smooth thromboresistant finish.

NIH Catheter TheNIH(NationalInstitutesofHealth)catheter is designed with a thin wall and nylon core construction to provide maximum flow rates and catheter stability.The flexible tip makes positioning in the cardiopulmonary system easier. This catheter is used to visualize the aorta, ventricles, pulmonary vasculature and the great veins.General Characteristics:• Nylon core• Closed end• Six sideholes

Pediatric NIH CatheterThis thin-walled catheter is designed to provide maximum flow and flexibility. The catheter can be used for aortic, ventricular, pulmonary and large-vein contrast studies.General Characteristics:• Closed end• Six sideholes (4 F catheter has four

sideholes)• Thin-wall construction

Lehman® Ventriculography CatheterJ.S. Lehman, MD, developed the Lehman®

ventriculography catheter. This catheter is specifically designed to be placed easily into the left ventricle via the aorta. The flexible, tapered distal tip is slightly curved to assist passage through the aortic valve and to sit freely in the contour of the left ventricle. The location of the four sideholes enables the angiographer to record proximal aortic pressures without removing the tip from the aortic valve. This catheter provides excellent flow rates and catheter stability due to its thin-wall construction.General Characteristics:• Closed end• Four sideholes• Thin-wall construction

Gensini® Percutaneous CatheterGoffredo G. Gensini, MD, is responsible for the first designed catheter with an open end hole. This catheter has a tapered tip that fits securely over a guidewire for percutaneous introduction. The six sideholes and thin-wall construction provide maximum flow rates. The catheter is used for aortic, ventricular, pulmonary and large-venous contrast studies.General Characteristics:• Open end• Six sideholes• Thin-wall construction

General Characteristics:Supplied sterile.items per box: 10 (Note: 5 per box for Cardio-Marker image band models)

Product Code French Size Design Style Length (cm)

001348 5 Thin wall 50001353 6 Thin wall 80001358 7 Thin wall 100001359 7 Thin wall 125

Product Code French Size Design Style Sideholes Length (cm)

001375 4 Thin wall 4 50 001377 5 Thin wall 6 50001378 5 Thin wall 6 80001380 6 Thin wall 6 50001381 6 Thin wall 6 80001382 6 Thin wall 6 100


010010* 5 Thin wall 65010011* 6 Thin wall 80010012* 7 Thin wall 80

*Items per box: 5

Pediatric NIH

Pediatric NIH with Cardio-Marker Image Bands Bandwidth: 1 mm; two marker bands 1 cm apart ±0.5 mm (leading edge to leading edge)

NIH


008761 5 Thin wall 65008762 6 Thin wall 65008763 7 Thin wall 80

Product Code French Size Design Style Length (cm) Comments

001415 7 Thin wall 100 Closed end

Product CodeFrench

Size Design StyleMinimum Tip

I.D. (in.)Length

(cm) Comments001323 5 Thin wall 0.026 100 Use with 0.025" guidewire001339 6 Thin wall 0.036 80 Use with 0.035" guidewire

Pediatric Curved NIH

Lehman Ventriculography

Gensini Percutaneous Catheter

84





Pediatric product.

woven Coronary Catheters—General Purpose and Transvalvular Catheters

Lehman® Catheter

J.S. Lehman, MD, designed a catheter for right heart studies similar to the Cournand catheter. The Lehman catheter has a thin-wall construction that maximizes catheter flexibility and flow rates.

General Characteristics:• Open end• No sideholes• Thin-wall construction

thin wall

Standard wall

Product Code French Size Design StyleMinimum Tip I.D.

(in.) Length (cm)001433 6 Standard wall 0.036 100001434 6 Standard wall 0.036 125007455 7 Standard wall 0.046 100007456 7 Standard wall 0.046 125


(in.) Length (cm)001253 5 Thin wall 0.032 50001254 5 Thin wall 0.032 80001263 7 Thin wall 0.055 100001264 7 Thin wall 0.055 125


(in.) Length (cm)001279 5 Thin wall 0.032 80001453 5 Standard wall 0.026 50001284 6 Thin wall 0.043 100001288 7 Thin wall 0.055 100007459 7 Standard wall 0.046 100007460 7 Standard wall 0.046 125

Cournand Catheter

Lehman Catheter

Goodale-Lubin Catheter

The general construction of these catheters consists of a woven outer core and a high-density polyurethane coating.

Cournand® Catheter

Designed by Andre Cournand, MD, in 1939, this catheter was the first to be manufactured specifically for use in the heart. The gradually curved tip facilitates easy access to the right heart. The Cournand® catheter is used for blood sampling and pressure measurements.

General Characteristics:• Open end• No sideholes• Standard wall construction

Goodale-Lubin® Catheter

Walter T. Goodale, MD, and Martin Lubin, MD, developed standard-wall and thin-wall catheters similar to the Cournand and Lehman catheters in construction and tip curve. The additional feature of the Goodale-Lubin catheter is the two laterally opposed sideholes just proximal to the tip for improved disbursement of contrast during right heart angiography.

General Characteristics:• Open end• Two laterally opposed sideholes• Thin-wall or standard-wall construction


85

Input® TS Introducer Sheaths

Product Code French SizeObturator Included Color Code

Length (cm)

Dilator Length (cm)

wire Style (in.)

040028A 5 No Gray 7 13 0.038 DDJ040031A 6 No Green 7 13 0.038 DDJ040035A 7 No Orange 7 13 0.038 DDJ051101A 5 No Gray 11 17 0.038 DDJ061101A 6 No Green 11 17 0.038 DDJ071101A 7 No Orange 11 17 0.038 DDJ081101A 8 No Blue 11 17 0.038 DDJ091101A 9 No Gray 11 17 0.038 DDJ010101A 10 No Dk Blue 11 17 0.038 DDJ011101A 11 No Red 11 17 0.038 DDJ060037A 6 Yes Green 23 29 N/A070037A 7 Yes Orange 23 29 N/A080037A 8 Yes Blue 23 29 N/A090037A 9 Yes Gray 23 29 N/A


Length (cm)

Dilator Length (cm)

wire Style (in.)

051102A 5 11 7 18 17 0.038 DDJ061102A 6 11 7 18 17 0.038 DDJ071102A 7 11 7 18 17 0.038 DDJ081102A 8 11 7 18 17 0.038 DDJ091102A 9 11 7 18 17 0.038 DDJ

Input TS Introducer Sheath

Input TS Introducer Sheath with Needle and Guidewire

• FEP sheath with silicone coating.

• Silicone hemostasis valve.

• Polyethylene dilator with silicone coating. Double distal “J” stainless steel guidewire (included in 7-cm and 11-cm sheaths only).

• See obturators, dilators and sterile sleeves.

input tS introducer sheath dilator

input tS introducer sheath

input tS introducer sheath with dilator

General Characteristics:Supplied sterile.Maximum guidewire: 0.038"items per box: 5

5 F 6 F 7 F 8 F 9 F 10 F 11 F

Color Code for Introducer French Sizes




Introducers

86




Introducers

Input PS Introducer Sheath

Available in Angio-Kits and EZ-Pak® kits.

Input PS Introducer Sheath with Needle and Guidewire


• Pebax® sheath.• Silicone hemostasis valve.• Polyethylene dilator.• Double distal “J” stainless steel.

guidewire (included in 11-cm sheaths only).

• HydroPel®hydrophiliccoating:water-activated, super lubricious coating on the distal portions of the sheath assembly.

• See obturators, dilators, sterile sleeves and Tuohy-Borst locking device.


Length (cm)

Dilator Length (cm)

wire Style (in.)

050011 5 No Gray 11 17 0.038 DDJ060011 6 No Green 11 17 0.038 DDJ070011 7 No Orange 11 17 0.038 DDJ080011 8 No Blue 11 17 0.038 DDJ090011 9 No Gray 11 17 0.038 DDJ060023 6 Yes Green 23 31 N/A070023 7 Yes Orange 23 39 N/A080023 8 Yes Blue 23 39 N/A090023 9 Yes Gray 23 39 N/A853311 5 No Gray 11 17 N/A863311 6 No Green 11 17 N/A873311 7 No Orange 11 17 N/A883311 8 No Blue 11 17 N/A893311 9 No Gray 11 17 N/A

Product Code French SizeLength

(cm)Needle Length

(cm)Needle Gauge

Dilator Length (cm)

wire Style (in.)

553311 5 11 7 18 17 Gray563311 6 11 7 18 17 Green573311 7 11 7 18 17 Orange583311 8 11 7 18 17 Blue593311 9 11 7 18 17 Gray

Input® PS Introducer Sheaths

General Characteristics:Supplied sterile.Maximum guidewire: 0.038"items per box: 5

87

C O R O N A R Y



introducersDiagnostics and Accessories—Introducers

Input PS Introducer Sheath Obturator

Input TS Introducer Sheath Obturator

input introducer sheath short (11 cm) obturator

input introducer sheath long (23 cm) obturator

Input® Accessories

• Color-coded for easy identification of compatible sheath.• Helpsmaintainsheathpatencyandprotectsfromoutside

contamination.• Twist’N Shut locking system locks obturator in place to prevent

backout from sheath.• Inserted into the introducer sheath when placement of the

transvenous temporary pacing electrode or intravascular catheter is delayed or removed.

Product Code Use with Introducer Obturator Included Obturator Length (cm) O.D. (in.)205211 050011 Gray 11 0.057206211 060011 Green 11 0.065207211 070011 Orange 11 0.078208211 080011 Blue 11 0.091209211 090011 Gray 11 0.104206223 060023 Green 23 0.065207223 070023 Orange 23 0.078208223 080023 Blue 23 0.091209223 090023 Gray 23 0.104

Product Code Use with Introducer Obturator Included Obturator Length (cm) O.D. (in.)205211A 051101A Gray 11 0.057206211A 061101A Green 11 0.065207211A 071101A Orange 11 0.078208211A 081101A Blue 11 0.091209211A 091101A Gray 11 0.104206223A 060037A Green 11 0.065207223A 070037A Orange 11 0.078208223A 080037A Blue 11 0.091209223A 090037A Gray 11 0.104

Obturators

Input PS Introducer Sheath Vessel Dilator

Input TS Introducer Sheath Vessel Dilator

• For use in arterial or venous applications.

• Polyethelyne dilator.

Product Code French Size Color Code Maximum wire Size (in.) Length (cm)653311 5 Gray 0.038 17663311 6 Green 0.038 17673311 7 Orange 0.038 17683311 8 Blue 0.038 17693311 9 Gray 0.038 17663323 6 Green 0.038 31673323 7 Orange 0.038 Double 39683323 8 Blue 0.038 Double 39693323 9 Gray 0.038 Double 39

Product Code French Size Color Code Maximum wire Size (in.) Length (cm)040037A 5 Gray 0.038 17040042A 6 Green 0.038 17040044A 7 Orange 0.038 17040047A 8 Blue 0.038 17040049A 9 Gray 0.038 17

Vessel Dilators

Sterile Sleeves for Use with Input Introducer Sheaths

• Maintains sterility of indwelling catheter shaft proximal to the introducer hub.

• Twist ‘N Shut locking system locks sleeve into input hub.

input introducer sheath sterile sleeve

Product Code Length (cm)026000 26060000 60


88




Introducers

• Sheath length 13 cm

• Dilator length 20 cm

• Split-away sheath with valve and side port

Input® SSV Split-Away Sheath with Valve and Side Port

• The Input SSV introducer incorporates all the benefits of a hemostasis valve into a split-away sheath.

• The Input SSV Introducer allows you to exchange leads with minimal blood loss.

Product Code French SizeSheath Length

(cm)Dilator Length

(cm)808600 6 13 20808700 7 13 20808800 8 13 20808900 9 13 20808950 9.5 13 20808100 10 13 20808150 10.5 13 20808110 11 13 20808120 12 13 20


89

C O R O N A R Y



introducersDiagnostics and Accessories—Introducers

Transseptal Catheter Introducer Sheaths

Mullins Transseptal Cath-eter Introducer Sheath

Mullins Transseptal Cath-eter Introducer Sheath—Pediatric

For use with pediatric Brockenbrough needle, product codes 003997 and 003996.

Sets include one sheath and one dilator. Use with Brockenbrough® needle, except where noted.

Mullins transseptal catheter introducer sheath

Product Code French SizeMaximum wire Size

(in.)Sheath Length

(cm)Dilator Length

(cm)008550 6 0.032 59 67008551 7 0.032 59 67008552 8 0.032 59 67



(in.)Sheath Length

(cm)Dilator Length

(cm)008530 6 0.025 44 52008531 7 0.025 44 52008532 8 0.025 44 52

Pediatric product.

For use with Brockenbrough needle, product codes 003994 and 003993.

90




Introducers

Transseptal Catheter Introducer Sheath with Hemostasis Valve

For use with Brockenbrough needle, prod-uct code no. 003994.

Set includes one sheath and one dilator. Used with Brockenbrough® needle.

Transseptal catheter introducer sheath has attached sidearm with stopcock and hemostasis valve.


(in.)Sheath Length

(cm)Dilator Length

(cm)008591 8 0.032 59 67


91

Product Code Description Packaged with

AC2200 Everest20 inflation device 1 three-way stopcock

AC3200 Everest30 inflation device 1 three-way stopcock

Product Code Description Packaged with

AC2205P Everest20 survival kit 1 Everest20 atm inflation device, 1 three-way stopcock, Piton Y-adapter, guidewire insertion tool, and steering handle

AC3205P Everest30 survival kit 1 Everest30 atm inflation device, 1 three-way stopcock, Piton Y-adapter, guidewire insertion tool, and steering handle

Everest Inflation Device

Everest Inflation Device

Everest Survival Kit

• Available with a three-way stopcock.

• The pistol-grip fits comfortably in either hand.

• A 20-cc syringe capacity provides rapid negative pressures to speed deflation times.

• The 20 atm/bar and 30 atm/bar luminescent gauges are easy to read under normal and low-ight conditions.

General Characteristics:Supplied sterile.items per box: 1Kits per box: 1


Interventional Accessories


© 2011 Medtronic, Inc. All rights reserved. UC200104306dEN 9/11

92


© 2011 Medtronic, Inc. All rights reserved. UC200104306dEN 9/11


Interventional Accessories


Piton Y-Adapter

Insertion tool

Piton Y-Adapter

Insertion tool

Steering handle

Piton Tri-Adapter

Insertion tool

Product Code Color Lumen I.D. (in.)

AC4001M Clear/Blue 0.110


AC4003M — 0.110


AC4002M — 0.110

Piton Y-Adapter

Piton Y-Adapter Kit

Piton Tri-Adapter

Piton® Disposable Adapters

Package includes:• One Piton Y-Adapter• One insertion tool

Kit includes:

• One Piton® Y-Adapter

• One insertion tool

• One steering handle

Package includes:

• One Piton Tri-Adapter

• One insertion tool

Stretch Insertion ToolStretch insertion tool for use with Piton Y-Adapter and Piton Tri-Adapter.

Product Code

006073

Product Code

008958

Product Code

AC4006

Steering Handles

Steering Handle for Use with PTCA Guidewires Plastic nut with metal jaws.

PTCA Guidewire Steering HandleAlso available kitted with Everest inflation device and Piton Y-Adapters.

93

General Characteristics:Supplied sterile.items per box: 10Maximum guidewire equals minimum tip I.D.


Pediatric Products

General Characteristics:Supplied sterile.items per box: 10Maximum guidewire equals minimum tip I.D.


Pediatric Products

Pediatric woven Coronary Catheters

Product CodeFrench

Size Design StyleMinimum Tip

I.D. (in.) SideholesLength

(cm) Comments

001323 5 Thin wall 0.026 6 100Use with 0.025"

guidewire

001339 6 Thin wall 0.036 6 80Use with 0.035"

guidewire

Gensini® Percutaneous Catheter

thin wall Standard wall

Product CodeFrench

Size Design StyleMinimum Tip I.D.

(in.) Sideholes Length (cm)

001279 5 Thin wall 0.032 2 80

001453 5 Standard wall 0.026 2 50

Goodale-Lubin® Catheter

Product CodeFrench

Size Design StyleMinimum Tip I.D.

(in.) Sideholes Length (cm)

001253 5 Thin wall 0.032 No sideholes 50

001254 5 Thin wall 0.032 No sideholes 80

Lehman® CatheterJ. S. Lehman, MD, designed the Lehman ventriculography catheter. This catheter is specifically designed to be placed easily into the left ventricle via the aorta. The flexible, tapered distal tip is slightly curved to assist passage through the aortic valve and to sit freely in the contour of the left ventricle. This catheter provides stability due to its thin-wall construction.

General Characteristics:• No sideholes• Thin-wall construction

The general construction of these catheters consists of a woven outer core and a high-density polyurethane coating.

Goffredo G. Gensini, MD, is responsible for the first designed catheter with an open-end hole. This catheter has a tapered tip that fits securely over a guidewire for percutaneous introduction. The six sideholes and thin-wall construction provide maximum flow rates. The catheter is used for aortic, ventricular, pulmonary and large-venous contrast studies.

General Characteristics:

• Open end• Six sideholes• Thin-wall construction

Walter T. Goodale, MD, and Martin Lubin, MD, developed standard-wall and thin-wall catheters similar to the Cournand and Lehman catheters in construction and tip curve. The additional feature of the Goodale-Lubin catheter is the two laterally opposed sideholes just proximal to the tip for improved disbursement of contrast during right heart angiography.

General Characteristics:• Two laterally opposed sideholes• Thin-wall or standard-wall construction

Pediatric product.



94



General Characteristics:Supplied sterile.items per box: 10 (Note: 5 per box for Cardio-Marker Image Band models)Maximum guidewire equals minimum tip I.D.


Pediatric Products

General Characteristics:Supplied sterile.items per box: 10 (Note: 5 per box for Cardio-Marker Image Band models)Maximum guidewire equals minimum tip I.D.Pediatric woven NIH Catheters

Pediatric product.

High-volumeangiographiccathetersdesignedtofacilitatelarge-volumecontraststudies.Theconstructionstyleconsists of a woven outer core and a polyurethane buildup with a smooth thromboresistant finish.

TheNIH(NationalInstitutesofHealth)catheterisdesigned with a thin wall and nylon core construction to provide maximum flow rates and catheter stability.The flexible tip makes positioning in the cardiopulmonary system easier. This catheter is used to visualize the aorta, ventricles, pulmonary vasculature and the great veins.

General Characteristics:• Nylon core• Closed end• Six sideholes• Thin-wall construction

This thin-walled catheter is designed to provide maximum flow and flexibility. The catheter can be used for aortic, ventricular, pulmonary and large-vein contrast studies.

General Characteristics:• Nylon core• Closed end• Six sideholes (4 F catheter has four sideholes)• Thin-wall construction

This thin-walled catheter is designed to provide maximum flow and flexibility. The catheter can be used for aortic, ventricular, pulmonary and large-vein contrast studies.

General Characteristics:• Nylon core• Closed end• Six sideholes • Thin-wall construction


001348 5 Thin wall 6 50

001353 6 Thin wall 6 80


001375 4 Thin wall 4 50 001377 5 Thin wall 6 50001378 5 Thin wall 6 80001380 6 Thin wall 6 50001381 6 Thin wall 6 80001382 6 Thin wall 6 100


010010* 5 Thin wall 6 65010011* 6 Thin wall 6 80010012* 7 Thin wall 6 80

*Items per box: 5

Pediatric NIH Catheter

Pediatric NIH with Cardio-Marker Image Bands This thin-walled catheter is designed to provide maximum flow and flexibility. The catheter can be used for aortic, ventricular, pulmonary and large-vein contrast studies.Bandwidth: 1 mm; two marker bands 2 cm apart ±0.5 mm (leading edge to leading edge)

NIH


008761 5 Thin wall 6 65008762 6 Thin wall 6 65008763 7 Thin wall 6 80

Pediatric Curved NIH

95





Pediatric Products


• Woven shaft design• Shaft length: 50 cm

• Woven shaft design• Shaft length: 50 cm

Rashkind Balloon Cath-eter—Single Lumen

Rashkind Balloon Cath-eter—Double Lumen

Product Code Shaft French SizeRecommended Inflated Balloon Diameter (mm)

Recommended Introducer (F) Comments

007161 4 11 7 Single lumen

007160 5 12 8 Single lumen

Product Code Shaft French SizeRecommended Inflated Balloon Diameter (mm)

Recommended Introducer (F) Comments

007158 5.5 14 9 Double lumen

Pediatric Rashkind® Septostomy Balloon Catheters

Pediatric product.

96



General Characteristics:not supplied sterile.items per box: 1

Brockenbrough needles and accessories are made of stainless steel.

The Brockenbrough needle is used with the Pediatric Mullins Transseptal Catheter Introducer Sheath to perform the transseptal technique.

This needle set includes one curved and one straight needle.

The Brockenbrough needle is used with the Pediatric Mullins Transseptal Catheter Introducer Sheath.

Brockenbrough curved needle

Brockenbrough Needle Set

Brockenbrough Curved NeedleTo be used with the Pediatric Mullins Transseptal Catheter Introducer Sheath.

Brockenbrough curved needleBrockenbrough straight needle

Pediatric Mullins Transseptal Introducer Sheath

For use with pediatric Brockenbrough needle, product codes 003997 and 003996.

Set includes one sheath and one dilator.

Brockenbrough® Needles

Product Code Size Length (cm)

003997 19 gauge 56

Product Code Size Length (cm)

003996 19 gauge 56


(in.)Sheath Length

(cm)Dilator Length

(cm)008530 6 0.025 44 52008531 7 0.025 44 52008532 8 0.025 44 52

General Characteristics:Supplied sterile.Maximum guidewire is 0.025"items per box: 1

Pediatric product.


Pediatric Products


Hemodynamic Monitoring Catheter

97

Pulmonary wedge Pressure (PwP) Catheter

Balloon inflation 1.5 cc

• Provides placement for hemodynamic pressure readings.

• Large lumen for blood sampling and pressure tracings.

• Accommodates 0.038" guidewire.

• Packaged with balloon inflation syringe.

Product Code French Size Length (cm)

150075 7 110

General Characteristics:Supplied sterile.For single use.Maximum guidewire: 0.038"items per box: 5


© 2011 Medtronic, Inc. All rights reserved. UC200104309cEN 9/11

98




Hemodynamic Monitoring Catheters

99

Product Code Size (in./mm) Length (cm) Comments

007873 0.038/1.0 45 Standard taper core 6 cm008879 0.021/0.5 15 Standard taper core 6 cm010439 0.025/0.6 45 Standard taper core 6 cm010440 0.035/0.9 45 Standard taper core 6 cm

Straight Tip: Fixed Core

General Characteristics:Supplied sterile.Packaged in coiled hoops.items per box: 10



Spring coil

Handle

Core wire

Safety wire

J Tip fixed core

J Tip movable core

Stainless Steel Guidewires

Fixed core

Spring coil Core wire Safety wire

Movable core

Angiography guidewires are available in two core designs, fixed and movable:

Fixed core: has a gradually tapered core.

Movable core: allows the wire softness to be adjusted manually by moving the core wire back and forth, allowing the operator to lengthen or shorten at will.

Coatings: Angiography guidewires are available with a PTFE coating applied over the entire core, enabling free movement and a smooth sliding action. PTFE wires are available with or without heparin coating.

Tips: A unique J Tip configuration is available on both the fixed and movable core wires. This J Tip can be “fingertip-straightened” from virtually any point of the wire shaft. This built-in convenience eliminates the need for a J straightening tool for wire loading.

Medtronic offers a variety of tip configurations, sizes and styles. The two most common tip configurations are straight and ‘‘J.”

Medtronic guidewires are available in a range of diameters and are compatible with the following minimal needle sizes:

Guidewire Diameter (in./mm) Minimum Needle Size

0.025/0.6 19 gauge0.032/0.8 18 gauge0.035/0.9 18 gauge0.038/1.0 18 gauge0.045/1.1 16 gauge


007874 0.025/0.6 45 Standard taper core 6 cm007875 0.035/0.9 45 Standard taper core 6 cm

3-mm J Tip: Fixed Core


008529 0.035/0.9 45 Double distal spring 3 cm

3-mm J Tip: Movable Core

Hemodynamic Monitoring CathetersDIAGNOSTICS AND ACCESSORIES

Angiographic Guidewires

100






Product Code Size (in./mm) Length (cm) Comments010388 0.025/0.6 145 Standard taper core 6 cm008952 0.028/0.7 145 Standard taper core 6 cm008953 0.032/0.8 145 Standard taper core 6 cm007041 0.035/0.9 120 Standard taper core 6 cm007042 0.035/0.9 145 Standard taper core 6 cm008627 0.035/0.9 175 Standard taper core 6 cm007044 0.038/1.0 145 Standard taper core 6 cm008628 0.038/1.0 175 Standard taper core 6 cm010003 0.035/0.9 145 Long taper core 10 cm010004 0.038/1.0 145 Long taper core 10 cm


PTFE-Coated Guidewires: Fixed Core

Product Code Size (in./mm) Length (cm) Comments008944 0.035/0.9 175 Rosen guidewire008945 0.038/1.0 175 Rosen guidewire

1.5-mm J Tip: Fixed Core

Product Code Size (in./mm) Length (cm) Comments007468 0.035/0.9 145 Extra-long taper core 15 cm007643 0.038/1.0 145 Extra-long taper core 15 cm007467 0.035/0.9 145 Long taper core 10 cm007642 0.038/1.0 145 Long taper core 10 cm007641 0.025/0.6 120 Standard taper core 6 cm010387 0.025/0.6 145 Standard taper core 6 cm007644 0.032/0.8 120 Standard taper core 6 cm007645 0.032/0.8 145 Standard taper core 6 cm007045 0.035/0.9 120 Standard taper core 6 cm007046 0.035/0.9 145 Standard taper core 6 cm008629 0.035/0.9 175 Standard taper core 6 cm007048 0.038/1.0 145 Standard taper core 6 cm








101






PTFE-Coated Guidewires: Movable Core

Heparin over PTFE-Coated Guidewires (Fixed Core and Movable Core)

Product Code Size (in./mm) Length (cm)

007647 0.032/0.8 145007051 0.035/0.9 145007053 0.038/1.0 145

Straight Tip: Movable Core





007648 0.032/0.8 120007649 0.032/0.8 145007446 0.035/0.9 120007447 0.035/0.9 145007054 0.038/1.0 145



008438 0.035/0.9 145 Standard taper core 6 cm008440 0.038/1.0 145 Standard taper core 6 cm020003 0.035/0.9 145 Long taper core 10 cm020004 0.038/1.0 145 Long taper core 10 cm



007445 0.035/0.9 145



008441 0.035/0.9 145008439 0.038/1.0 145


102





General Characteristics:Supplied sterile.Packaged in coiled hoops.

Specialty Guidewires

Straight Tip Exchange wire: Fixed CorePTFE-coated. Items per box: 10



PTFE-Coated 0.063" Guidewire: Fixed CoreFor placement of guiding catheter (flexible distal tip).

PTFE-coated. Items per box: 1

Product Code Tip Diameter (in.) Length (cm)

008418 6 mm “J” 0.063 160

Removable Luer Lock Hub For use with Sos open-ended guidewire (above). Product Code Size (in./mm) Comments

006210 Fits all sizes For use with Sos open-ended guidewire

Movable/removable core wire is packaged with removable luer lock hub, product code 006210 (shown below).

Sos open-ended guidewire has a clear PTFE outer jacket.

Items per box: 10

.038" OEGW

.035" OEGW

100 200 300 400 500 600

6

4

2

Pressure (PSi)

Flow

rat

e (c

c / s

ec)

Sos Open-Ended Guide-wire


006203 0.035/0.9 145 Standard taper core 6 cm006200 0.038/1.0 145 Standard taper core 6 cm006204 0.035/0.9 145 Long taper core 10 cm006201 0.038/1.0 145 Long taper core 10 cm

3-mm J Tip Exchange wire: Fixed CorePTFE-coated. Items per box: 10



103





General Characteristics:Supplied sterile.Packaged in coiled hoops.

SoftwirePtFe-coated. items per box: 10


006305 0.035/0.9 145 Extra-long taper core 15 cm006307 0.038/1.0 145 Extra-long taper core 15 cm

Flexible tip

Steering HandlePtFe-coated. items per box: 5

Product Code Comments

006854 For use with 0.035"/0.038" guidewires

Steerable Guidewire with Steering HandlePtFe-coated. items per box: 5


010037 0.035/0.9 145 3-cm flexible tip010038 0.038/1.0 145 3-cm flexible tip

Specialty Guidewires, continued

104





105



Brockenbrough needles and accessories are made of stainless steel.

Brockenbrough curved needle

Brockenbrough Curved NeedleThe Brockenbrough needle is used with one of the following transseptal products to perform the transseptal technique: • Mullins transseptal catheter

introducer sheath• Transseptal catheter introducer

sheath

Brockenbrough® Needles

Product Code Size Length (cm) Comments

003994 18 gauge 71 To be used with either transseptal catheter introducer sheath

003997 19 gauge 56To be used with the pediatric Mullins transseptal catheter

introducer sheath

General Characteristics:not supplied sterile.items per box: 1

Pediatric product.

Transseptal Catheter Introducer Sheaths

Mullins Transseptal Catheter Introducer Sheaths—Pediatric


Set includes one sheath and one dilator. Used with Brockenbrough needle, except where noted.

Mullins transseptal catheter introducer sheath



(in.)Sheath Length

(cm)Dilator Length

(cm)008530 6 0.025 44 52008531 7 0.025 44 52008532 8 0.025 44 52

This needle set includes one curved and one straight needle.

Brockenbrough Needle Set

Brockenbrough curved needleBrockenbrough straight needle

Product Code Size Length (cm) Comments

003993 18 gauge 71 To be used with either transseptal catheter introducer sheath

003996 19 gauge 56To be used with the pediatric Mullins transseptal catheter

introducer sheath

Mullins Transseptal Catheter Introducer Sheath


(in.)Sheath Length

(cm)Dilator Length

(cm)008550 6 0.032 59 67008551 7 0.032 59 67008552 8 0.032 59 67



Transseptal Products

106




Transseptal Products

Transseptal Catheter Introducer Sheath with Hemostasis Valve

For use with Brockenbrough needle, product code 003994.

Set includes one sheath and one dilator. Used with Brockenbrough® needle.

Transseptal catheter introducer sheath has attached sidearm with stopcock and hemostasis valve.

Product Code French Size Maximum wire Size (in.) Sheath Length (cm) Dilator Length (cm)

008591 8 0.032 59 67


107

Contact and Ordering Information

Reimbursement Medtronic’sHealthcareEconomicsteamisdedicatedtoeducatingcustomersonproductcoding,coverageand reimbursement. It ensures that customers make economically efficient use of our products and submit timelyandaccurateclaimsforservicestheyperform.The HealthcareEconomicsProgramprovidesatoll-freecoding hotline weekdays from 8 a.m. to 5 p.m. CST as well as web seminars on pertinent industry topics.

Vascular Reimbursement Information LinePhone: 707.591.7869

Technical Support LifeLine Customer Support is a first point of contact for rapid turnaround to customers’ technical questions and needs. Support services include expertise in objection handling, product specifications and use, patient education and no cross.

For product information, contact: LifeLine CardioVascular Technical Support Phone: 877.526.7890 Alternate phone: 763.526.7890 Fax: 763.526.7888 Technical specialists are available weekdays from 7:30 a.m. to 6 p.m. CST. Emergency service is available 24/7 outside of normal full-service hours.

Ordering To order products, contact: Medtronic Product Services Phone: 888.283.7868 Fax: 800.838.3103

Mailing address: Medtronic, Inc. CardioVascular Customer Care 800 - 53rd Ave. NE ColumbiaHeights,MN55421 Customer Care specialists are available weekdays from 7 a.m. to 7 p.m. CST.

Emergency service is available outside of normal full-service hours.

Shipping Medtronic will incur all shipping charges. Standard delivery is ground, but shipping can be upgraded upon request. If product is damaged in shipment, obtain a claim inspection report from the carrier within 15 days.

Pricing and Terms Prices are subject to change without prior notice. Payment is required within net 30 days of invoice. Please contact Customer Care for questions regarding remittance for your ZIP code.

Return Policy Authorization must be obtained from your Medtronic sales representative or Customer Care specialist before product is returned. Please be prepared with the reason for return, model, lot number, quantity and original purchase order (PO). The Returned Goods Authorization (RGA) number must be clearly identified on the carton of returned product. Product may be subject to a 20% restocking fee. Merchandise processed in error by Medtronic will be credited in full.

Note: Product availability and specifications are subject to change without notice.

108

Product Eligible Product must be:for Return • Within90daysofinvoice. • Inunopened,saleablecondition. • Anactivemodelincludedinthecurrentpricelist. • Aproductthathasnotreachedorexceededthe“use-before”date. • Acompleteboxorkit. • Astandardcatalogitem(specialbuildproductisnoteligibleforreturn).

Shipping Address Medtronic Inc. (RGA#)for Returns Attn: Return Finished Goods

4340 Swinea Road, Building AMemphis, TN 38118

Note: Product availability and specifications are subject to change without notice.

August 2011

Contact and Ordering information, continued

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Medtronic may not carry products used in all procedures listed. © 2011 Medtronic, Inc. All rights reserved. Printed in USA. UC201104888EN 2/11

Card

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CAUTION: Federal (USA) law restricts these devices to sale by or on the order of a licensed healthcare practitioner.

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For further information, please call and/or consult Medtronic at the toll-free numbers or websites listed below:

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