sanjay gandhi post graduate institute of medical...
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SANJAY GANDHI POST GRADUATE INSTITUTE OF MEDICAL SCIENCES
RAEBARELI ROAD, LUCKNOW-226014. PHONES:2668004-8,2668700,2668800,2668900
FAX: 91-522-2668973,2668218 (JDMM)
Email: [email protected] Sealed offers are invited from reputed manufacturer/ Direct Importer/ Accredited Agent for supply of the
following equipments, as per tender conditions as stipulated in the tender documents. Tender documents
duly filled in will be received by speed post / regd. Post / courier only in the RSD cell, 3rd floor,
Administrative block of the Institute in two bid system i.e. technical bid and price bid in separate
envelops. Then Both envelops may be sealed in single envelop. The tender no. and the name of the item
must be superscribed on the top of envelop. The tender fee Rs. 500.00+ Rs. 25.00 (VAT @ of 5%) Total Rs.
525.00 (Rs. Five Hundred Twenty Five Only) for each quoted item (Non refundable) along with the EMD
(Refundable) for respective tender(s) as indicated against each tender may be enclosed separately with
tender document in the shape of Demand Draft (Nationalized bank only) payable at Lucknow in favour of
the Director, SGPGIMS, Lucknow. Bids will be opened in the presence of authorized representative of the
bidders on scheduled date and time. If any working day is observed as holiday the next working day will
be treated as last date. In case any legal dispute, the legal jurisdiction shall be court of law at Lucknow
(UP), India.
Director reserves the right to accept or reject any tenders in part or full without assigning any reason
thereof. The institute will not be responsible for any postal delay.
Notice Inviting Tender Advertisement NO :I- 19/JDMM/2015-16
DIRECTOR
SL. NO.
TENDER NO. NAME OF EQUIPMENT QTY EMD LAST DATE OF SUBMISSION
DATE OF OPENING 11.00 AM ONWARDS
1. PGI/MM/CCM/15-16/03 ADULT AIRWAY MANAGEMENT TRAINER INTUBATION MANIKIN
01 5000.00 18.08.2015 TILL 4:00 PM
20.08.2015
2. PGI/MM/CCM/15-16/04 MANNEQUIN FOR CENTRAL VENOUS CATHETERIZATION FOR INTERNAL JUGULAR AND SUBCLAVIAN VEIN WITH ULTRASOUND GUIDANCE
01 5000.00 18.08.2015 TILL 4:00 PM
20.08.2015
3. PGI/MM/CVTS/15-16/03 STERNUM SAW 02 20000.00 18.08.2015 TILL 4:00 PM
20.08.2015
4. PGI/MM/NEO/15-16/01 BABY MANIKIN (NEONATAL) WITH INTUBATION HEAD
01 5000.00 18.08.2015 TILL 4:00 PM
20.08.2015
5. PGI/MM/NEO/15-16/02 FIBEROPTIC PHOTOTHERAPY UNIT 02 10000.00 18.08.2015 TILL 4:00 PM
20.08.2015
6. PGI/MM/RAD/15-16/01 CR CASSETTES COMPATIBLE WITH EXISTING FUJI CR
01 35000.00 18.08.2015 TILL 4:00 PM
20.08.2015
7. PGI/MM/TM/15-16/01 BLOOD BANK REFRIGERATOR (50-70 BAGS) CAPACITY WITH WIRELESS DATA LOGGER
10 15000.00 18.08.2015 TILL 4:00 PM
20.08.2015
8. PGI/MM/TM/15-16/02 REFRIGERATED CENTRIFUGE FOR COMPONENT SEPARATION
01 35000.00 18.08.2015 TILL 4:00 PM
20.08.2015
9. PGI/MM/TM/15-16/03 MULTI-HEAD TUBE SEALER (BENCH TOP)
01 5000.00 18.08.2015 TILL 4:00 PM
20.08.2015
10. PGI/MM/TM/15-16/04 BLOOD BANGS DISINFECTION SYSTEM (AUTOCLAVE)
01 5000.00 18.08.2015 TILL 4:00 PM
20.08.2015
11. PGI/MM/TM/15-16/05 PLASMA THAWING SYSTEM 01 5000.00 18.08.2015 TILL 4:00 PM
20.08.2015
12. PGI/MM/TM/15-16/06 DIELECTRIC TUBE SEALER (BENCH MODEL)
02 5000.00 18.08.2015 TILL 4:00 PM
20.08.2015
13. PGI/MM/TM/15-16/07 AUTOMATED SYSTEM FOR DETECTION FOR BACTERIA IN BLOOD COMPONENTS
01 10000.00 18.08.2015 TILL 4:00 PM
20.08.2015
14. PGI/MM/TM/15-16/08 STERILE CONNECTING DEVICE 02 20000.00 18.08.2015 TILL 4:00 PM
20.08.2015
15. PGI/MM/TM/15-16/09 BLOOD BAG TUBE STRIPPER 10 5000.00 18.08.2015 TILL 4:00 PM
20.08.2015
16. PGI/MM/NEPH/15-16/01 LARYNGOSCOPE 04 5000.00 18.08.2015 TILL 4:00 PM
21.08.2015
17. PGI/MM/NEPH/15-16/02 ELECTRONIC DIGITAL BP MEASUREMENT WITHOXYGEN PROBE SPO2 ON STAND
30 5000.00 18.08.2015 TILL 4:00 PM
21.08.2015
18. PGI/MM/NEPH/15-16/03 MULTIPARA MONITOR 04 25000.00 18.08.2015 TILL 4:00 PM
21.08.2015
19. PGI/MM/NEPH/15-16/04 DISSECTING MICROSCOPE 01 5000.00 18.08.2015 TILL 4:00 PM
21.08.2015
20. PGI/MM/NEPH/15-16/05 AUTOMATED ELECTRONIC ADJUSTABLE SPACER PIPPET
04 5000.00 18.08.2015 TILL 4:00 PM
21.08.2015
RE-TENDER
21. PGI/MM/PM/14-15/02 ENDOBRANCHIAL CRYO AND ARGON PLASMA COAGULATION SYSTEM
01 44000.00 18.08.2015 TILL 4:00 PM
21.08.2015
NEW TENDER
22. PGI/MM/PS/15-16/08 URODYNAMIC MACHINE 01 15000.00 18.08.2015 TILL 4:00 PM
21.08.2015
23. PGI/MM/PS/15-16/09 SURGICAL INSTRUMENTS 01 Set 5000.00 18.08.2015 TILL 4:00 PM
21.08.2015
24. PGI/MM/PS/15-16/10 ARGON PLASMA COAGULATION 01 15000.00 18.08.2015 TILL 4:00 PM
21.08.2015
25. PGI/MM/PG/15-16/02 BREATH ANALYZER, HYDROGEN AND METHANE ANALYZER
01 15000.00 18.08.2015 TILL 4:00 PM
21.08.2015
26. PGI/MM/PG/15-16/03 STATDIOMETER WITH INTEGRATED WEIGHING SCALE
02 4000.00 18.08.2015 TILL 4:00 PM
21.08.2015
27. PGI/MM/BIOSTAT/15-16/01
UPS (20 KVA) 02 11000.00 18.08.2015 TILL 4:00 PM
21.08.2015
28. PGI/MM/MS/15-16/02 REFRIGERATOR 60 5000.00 18.08.2015 TILL 4:00 PM
21.08.2015
29. PGI/MM/I.R.F./15-16/01 DEEP FREEZER -24 DEGREE 03 4000.00 18.08.2015 TILL 4:00 PM
21.08.2015
30. PGI/MM/MIS/15-16/01 SERVO VOLTAGE STABILIZER 02 10000.00 18.08.2015 TILL 4:00 PM
21.08.2015
31. PGI/MM/MIS/15-16/02 VOLTAGE STABILIZER 10 5000.00 18.08.2015 TILL 4:00 PM
24.08.2015
32. PGI/MM/HEMA/15-16/01 CARDIAC TRANSPORT MONITORS WITH ALL ACCESSORIES
10 35000.00 18.08.2015 TILL 4:00 PM
24.08.2015
33. PGI/MM/HEMA/15-16/02 DROP (VOLUMETRIC) INFUSION PUMP 15 9000.00 18.08.2015 TILL 4:00 PM
24.08.2015
34. PGI/MM/HEMA/15-16/03 DEFIBRILLATOR 01 3000.00 18.08.2015 TILL 4:00 PM
24.08.2015
35. PGI/MM/HEMA/15-16/04 ECG MACHINE 02 3000.00 18.08.2015 TILL 4:00 PM
24.08.2015
36. PGI/MM/HEMA/15-16/05 BEDSIDE ULTRASOUND MACHINE 01 18000.00 18.08.2015 TILL 4:00 PM
24.08.2015
37. PGI/MM/HEMA/15-16/06 ELISA READER 01 3000.00 18.08.2015 TILL 4:00 PM
24.08.2015
38. PGI/MM/HEMA/15-16/07 TISSUE FLOATATION BATH 01 3000.00 18.08.2015 TILL 4:00 PM
24.08.2015
39. PGI/MM/PATH/15-16/01 FROZEN SECTION FACILITY (CRYOSTAT)
01 25000.00 18.08.2015 TILL 4:00 PM
24.08.2015
40. PGI/MM/MICRO/15-16/02 REAL TIME PCR MACHINE 01 25000.00 18.08.2015 TILL 4:00 PM
24.08.2015
41. PGI/MM/MICRO/15-16/03 BIOMEDICAL WASTE COLLECTION BIN 40 4000.00 18.08.2015 TILL 4:00 PM
24.08.2015
42. PGI/MM/NM/15-16/01 INTERLOCK SYSTEM FOR WASTE GAS STORAGE TANK THROUGH RADIATION MONITORING DEVICES (CYCLOTRON FACILITY)
01 20000.00 18.08.2015 TILL 4:00 PM
24.08.2015
43. PGI/MM/NM/15-16/02 180 WATER PURIFIER SYSTEM (CYCLOTRON FACILITY)
01 30000.00 18.08.2015 TILL 4:00 PM
24.08.2015
44. PGI/MM/NM/15-16/03 WATER BATHS HEATING & RECIPROCAL SHAKING
01 1000.00 18.08.2015 TILL 4:00 PM
24.08.2015
45. PGI/MM/NM/15-16/04 ULTRAVIOLET VIEWING CABINET 01 2000.00 18.08.2015 TILL 4:00 PM
24.08.2015
46. PGI/MM/NM/15-16/05 LYPHOLYZER/FREEZE DRYER 01 5000.00 18.08.2015 TILL 4:00 PM
25.08.2015
47. PGI/MM/NM/15-16/06 HOT AIR HEATING AND DRYING OVEN (CYCLOTRON FACILITY)
01 2000.00 18.08.2015 TILL 4:00 PM
25.08.2015
48. PGI/MM/NM/15-16/07 CENTRIFUGE 01 2000.00 18.08.2015 TILL 4:00 PM
25.08.2015
49. PGI/MM/NM/15-16/08 ORGAN LEVEL INTERNAL DOSE ASSESSMENT (OLINDA) FOR THE INTERNAL DOSIMETRY
01 3000.00 18.08.2015 TILL 4:00 PM
25.08.2015
50. PGI/MM/NM/15-16/09 MICROWAVE SYNTHESIZER 01 20000.00 18.08.2015 TILL 4:00 PM
25.08.2015
51. PGI/MM/NM/15-16/10 PREPARATIVE FLASH CHROMATOGRAPHY SYSTEM (CYCLOTRON FACILITY)
01 30000.00 18.08.2015 TILL 4:00 PM
25.08.2015
52. PGI/MM/NM/15-16/11 INFUSION PUMP WITH LEAD SHIELDING
01 10000.00 18.08.2015 TILL 4:00 PM
25.08.2015
53. PGI/MM/CSSD/15-16/01 WHEELED BINS FOR HOSPITAL SANITATION (MATERIAL:HDPE)
222 15000.00 18.08.2015 TILL 4:00 PM
25.08.2015
54. PGI/MM/PH. T./15-16/01 ELECTROTHERAPY/ COMBINATION THERAPY
02 10000.00 18.08.2015 TILL 4:00 PM
25.08.2015
55. PGI/MM/PH. T./15-16/02 SHORT WAVE DIATHERMY 02 2000.00 18.08.2015 TILL 4:00 PM
25.08.2015
56. PGI/MM/PH. T./15-16/03 DECOMPRESSION THERAPY SYSTEM 01 20000.00 18.08.2015 TILL 4:00 PM
25.08.2015
57. PGI/MM/PH. T/15-16/04 GUTHERIE SMITH’S SUSPENSION FRAME
01 2000.00 18.08.2015 TILL 4:00 PM
25.08.2015
58. PGI/MM/PH. T./15-16/05 SHOULDER WHEEL EXERCISER 02 1000.00 18.08.2015 TILL 4:00 PM
25.08.2015
TENDER DOCUMENTS
TENDER DOCUMENTS & TERMS AND CONDITIONS
The following terms & conditions should be complied with while submitting tender:
1 Unconditional warranty & Guarantee for 5 yearsto be declared by OEM (Original Equipment Manufacturer)
from the date of installation.
2 An undertaking from the firm that the equipment is of the latest art technology and till date no revised or
amended version has been launched and the spare parts will remain available for at least next 10 years
3 The price bid should be in the following format:
Cost of equipment with warranty for 5 years declared by OEM and CMC after warranty period i.e. 6th
year to 10th
years from the date of installation, list of items not mentioned along with cost under CMC.
The L1 will be decided by adding the CMC of subsequent years.
4 Details of after sale service support.
5 List of installations in India should be provided with the tender documents.
6 Software upgradation, if needed, will be provided free of cost during warranty & CMC.
7 CMC will be 3% with spares with/without escalation or 5% with spares without escalation of subsequent year
must be undertaken. Please take this condition as mandatory where the rates of CMC have not been clarified in
that case the Institute will load 3% CMC without escalation and will be a binding on the firm.
8 The firm has to submit the copy of latest supply order for justification of quoted rates.
9 The firm will provide an affidavit to this effect that “THIS IS TO CERTIFY THAT THE RATES QUOTED
for……TO SGPGIMS, LUCKNOW ARE THE LOWEST ONE. WE HAVE NOT QUOTED/ SUPPLIED
AT LESSER PRICE TO ANY ORGANISATION WITH THESE SPECIFICATIONS. WE ALSO
DECLARE THAT ABOVE ITEMS HAVE BEEN/ ARE NOT SUPPLIED IN INDIA.
WE FURTHER AGREE THAT ANY PRICE DISCRIPANCY IS FOUND ON LATER DATE, WE
WILL BE LIABLE TO REFUND THE SAME.
10 Subletting of the tender to the sub-distributor is not permissible. If the same item is quoted by the principal
and the other two distributors in support, the same will be treated as pooling of tender and the firm would be
debarred from future business.
11 Tendersshould be submitted to the RSD Cell located at 3rd
Floor of the Administrative Building, Sanjay Gandhi
Postgraduate Institute of Medical Sciences, Raebareli Road, Lucknow 226014, India under the sealed cover
failing which the tender shall be disqualified.
12 The tender terms and conditions be clearly typed or legibly written giving the full name and address of the
tenderers. The tenderers should quote in figures as well as in words the rates and amount tendered by
him/them. Alteration, if any unless legibly attested by the tenderers, with their full signature, shall invalidate
the tender. The tender should be signed by the tenderers himself/themselves or his/their authorized agent on
his/their behalf. In case the tender is signed by the agent the authority letter in his favour shall be enclosed
with tender documents.
13 Sealed Tenders should be submitted in two-bid system (in two identical copies) consisting earnest money,
technical offer &price bid. In case of equipment tender the Earnest Money and Technical Bid shall be
submitted in first part i.e. technical bid and price be submitted in second part i.e. price bid both separately
sealed. The Price Bid should be in the following format:-
(a) Cost of equipment with warranty for 5 years declared by OEM.
(b) CMC cost after warranty period from 6th
year to 10th
years from the date of installation.
(c) List of item along with cost not covered under CMC. Any item not mentioned will be considered
part of warranty.
The L1 will be decided by adding the CMC cost of maximum up to 10 years.
14 The tenderers should take care that the rates and amounts are written in such a way that interpolation is not
possible. No blank space should be left, which would otherwise make the tender liable for rejection.
15 Delivery schedule with definite date of delivery at destination taking into cognizance of transit facilities must be
indicated. This contractual delivery date/period should be inclusive of all the lead-time.
16 The tenderers should clearly state whether he/they are manufacturer, accredited agents (declared by
manufacturer only), the name of Principal on the top of the Bid. The tender submitted through third party and
subletting of tender will not be entertained.
17 The tenderer submitting his tender would be deemed to have considered and accepted all the terms and
conditions. No Enquiries, verbal or written shall be entertained in respect of acceptance or rejection of the
tender.
18 The quantity shown in the schedule may be increase or decrease on any extent depending upon the actual
requirement.
19 The tenderer shall specify after sales services facilities within the Guarantee/Warrantee period. The warrantee
period will be extended for the period of the instruments remain out of order during warrantee period.
20 The tenderer shall also confirm the Installation, Commissioning, Demonstration and Training to the concerned
of this Institute.
21 The tenderer shall submit the pre-requisite information like Civil works/ Electrical details etc. All necessary
requirements along with the offer, in order to make the equipment functional. Any additional request made
after supply order will not be entertained and will be treated mandatory by default.
22 The Institute reserves the right to cancel/reject in full or any part of the tender which generally do not fulfill
the conditions stipulated in the tender without assigning any reason.
23 Any action on the part the tender to influence anybody of the Institute will make his tender liable to rejection.
24 The tenderers shall submit the offer with in original copy of the tender documents duly signed on each page.
Item-wise rates indicating units can be offered on letter head of the firm as indicates in Sl. no. 3 above.
25 In the case of placement of Purchase Order, the vendor (the tenderers whose tender is accepted) shall have to
confirm the purchase order within 7 days from the date of the dispatch of purchase order otherwise it will be
deemed that offer is acceptable to the firm. Notwithstanding any other provision, the terms & conditions and
any other items given in the Purchase order will be treated as binding with “Errors & omission Expected” basis.
However, if the supplier notices any mistake in the contentions of the order, he must bring the same to the
notice of the Institute and seek clarifications. Supplier will have to bear the responsibility for failure to take
this action.
26 The Institute may in writing make any revision or change in the purchase order, including additions or
deletions from the quantities originally ordered in the specifications or drawings. If any such revisions/changes
affect the price or delivery, the same shall be subject to the adjustment of price/delivery, where requires on a
reasonable basis by mutual agreement in writing which should be communicated.
27 The tenderer should furnish performance bank guarantee of 15% of the order value or FOB value at the time/
before shipment or supply of goods and this will be released after the successful completion of period
ofwarrantee i.e.5years. The PBG submitted will be valid for a period of 5 year from the date of installation.
28 The Institute reserves the right to cancel the purchase order or any part thereof and shall be entitled to revise
the contract wholly or in part by a written notice to the vendor, if :-
The vendor fails to comply with the terms of the purchase order including specifications and other technical requirement.
The vendor becomes bankrupt or goes into liquidation.
The vendor fails to deliver the goods in time and or does not replace the rejected goods promptly.
A receiver is appointed for any of the property owned by the vendor
29 Upon receipt of the said cancellation notice, the vender shall discontinue all works of the purchase order and
matters connected with it.
30 Earnest Money be paid in shape of D/D only drawn in favour of the Director, Sanjay Gandhi Postgraduate
institute of Medical Sciences and payable at Lucknow (U.P.), India as mentioned in the tender notification.
D/D should be from nationalized /scheduled bank.
31 Unless otherwise specified in the order, the order price shall remain firm and will not be subject to escalation
of any description during the pendency of the order, notwithstanding the change in the cost of materials,
labor and/or variations in taxes, duties and other levies on raw materials and components the may take place
while the order is under execution even if the execution of the order is delayed beyond the completion date
specified in the order for any reason whatsoever.
32 For indigenous goods the price should be on F.O.R. SGPGIMS Central Stores basis inclusive of all levies and
duties wherever applicable which should be indicated clearly. The rates of sales tax should be clearly indicated
wherever chargeable. The SGPGIMS is not eligible to issue ‘C’ or ‘D’ Form, however the concessional rate of
Central Sales Tax admissible to Research Institutions on purchase of Scientific Instruments/Equipments etc.
from certain States like Maharashtra., Delhi, West Bengal etc. is applicable to this Institute.
33 Prices will be quoted on FOB as well as estimated CIF SGPGI Central Stores (Insurance from firm’s
warehouse to SGPGI warehouse basis) for imported goods. Indian Agency commission / rebate payable to
Indian Agent, if any, shall be shown separately and that will be payable in equivalent rupee directly to
Indian Agent as per declaration furnished by foreign suppliers. The Institute reserves the right to get their
goods air-freighted/Sea freighted & air insured/marine insured upto site. The Indian Agency Commission
payable to Indian agent should be declared directly by the manufacture and not by Indian agent.
CUSTOM CLEARANCE: After arrival of the goods at Lucknow Airport, Indian agent or Indian subsidiary of the
principal firm is solely responsible for getting the material clearance from customs. Institute will provide all
custom documents for custom clearance on the demand of agent. Transportation from Air Port to SGPGI
Central Stores is also the responsibility of authorized agent. All charges/ expenses incurred in this process will
be reimbursed to firm after submitting the bill along with documentary proof in original. Please note that the
freight forwarder or clearing agent should be approved from IATA. NO DEMURRAGE / WHARFAGE CHARGES
WILL BE PAYBALE BY THE INSTITUTE UNDER ANY CIRCUMSTANCES. NO ADVANCE PAYMENT WILL BE
PAYABLE FOR CUSTOM CLERANCE/ FREIGHT / INSURANCE ETC. The certificate to this effect will be provided
that the rates charged are as per IATA. FIATA and does not contain any item other than ordered by the
Institute.
34 The offer of the tenders shall remain valid for a period of at least 180 days from the date of opening of the
tender.
35 All goods or materials shall be supplied by the tenderers whose tender is accepted, strictly in accordance with
the specifications, drawings, data sheets, other attachments and conditions stated any alterations of those
conditions shall not be made without the consent of the Institute in writing which must be obtained before
any work against the order is commenced.
All material furnished by the seller pursuant to this order (irrespective of whether engineering, design data or
other information has been furnished, reviewed or approved by the Institute) will be guaranteed to the best
quality of their respective kind (unless otherwise specifically authorized in writing by the Institute) and shall be
free from faculty design (to the extent such design is not furnished to the Institute) workmanship and
materials, and to be of sufficient size and capacity and of proper materials so as to fulfill in all respects with all
operating conditions, if any , specified in this order.
36 The Equipment supplied shall carry a standard warranty for 5 years (60 months)to be declared by OEM from
the date of satisfactory Installation and commissioning of the equipment. If any trouble or defect
originating with the design, materials, workmanship or operating characteristics of any materials arise at
any time from the date of Installation, the same shall promptly as possible make such alteration, repairs
and replacement as soon as notified thereof, the seller shall at his own expenses and as promptly as may be
necessary to permit the materials functionalinaccordance with the specification and to fulfill the foregoing
guarantee/ warranty and the Institute will enter into CMC agreement from six to ten year (6th
years to 10th
years) at the time of release of order which shall form the part of the order..
37 The Institute may at his option, remove such defective materials at the seller’s expense in which event the
seller shall, without any cost to the SGPGIMS and as promptly as possible, furnish and install proper materials,
repaired or replaced materials shall be similarly guaranteed for a period as per OEM not less than 12 (twelve)
months from the date of shipment.
38 In the event that the materials supplied do not meet the specifications and are not in accordance with the
drawings, data sheets or the terms of this order, rectification is required at site, the SGPIGMS shall notify to
the seller giving full details of differences. The seller shall attend the site, within seven days of receipt of such
notice to meet an agree with representative of the SGPGIMS the action required to correct the deficiency.
39 If the seller fails to attend meeting at site within the time prescribed above, the SGPGIMS shall immediately
get the same rectified the work/materials and seller shall reimburse the Institute all costs and expenses
incurred by the SGPGIMS in removing such trouble or defect.
40 100% payments shall be released within 30 days from the date of satisfactory receipt/installation of materials.
Where necessary performance bank guarantee @ 15% of the ordered value or FOB/order value shall be
submitted to the Institute before arranging the delivery till expiry of warranty period. Bank Guarantee be
submitted through bank only. In case of Imported goods/equipment, the payment schedule will be as
follows:-
90%will be released after shipment by negotiation.
10%will be released after satisfactory installation, commissioning & training under intimation to the Joint Director(MM) on issuance of certificate by the Institute.
41 The mode of payment will be through irrevocable letter of credit or International Bank draft. However, Indian
Agency Commission or Technical Service charges would be paid in Indian rupee after satisfactory receipt &
installation of goods at site duly verified by concerned HOD. Please note, in case of IBD, the original bank draft
will be handed over to firm only after satisfactory receipt and satisfactory installation of the equipment.
42 Time delivery as mentioned in Purchase order shall be the essence of the order and no variation shall be
permitted except with prior authorization in writing from Purchaser.
43 In the event of delay in making delivery on the part of the vendor, it will be at purchaser’s discretion to receive
delivery with a reduction in price of the article/ or equipment.
44 Forced majeure shall mean and be limited to the Following:
(a) Any war/hostilities. (b) Any riot or civil communication. (c) Any earthquake, flood tempest, lighting or other natural physical disaster (d) Any strike, or lock-out (only those exceeding ten continuous days in duration) affecting the
performance of the seller’s obligation.
45 The seller shall advise the SGPGIMS by e-mail, for and followed by registered letter duly certified by Local
Chamber of Commerce of Statuary authorities the beginning and end of the above causes of delay within 7
(seven) days of occurrence and cessation of such Forced Majeure conditions, in the event of delay lasting over
one month, if arising our causes of Force Majeure, the SGPIGMS reserves the right to cancel the order and the
provisions governing termination state under articles shall apply.For delays arising out of Forced Majeure, the
seller shall not claim extension in completion date for a period exceeding the period of delay attributable to
the causes of Force Majeure and neither the SGPGIMS nor the seller shall be liable to pay extra costs provided
it is mutually established that Force Majeure conditions did actually exist.The seller shall categorically specify
the extent of Force Majeure conditions prevalent in his works (such as power restriction etc.) at the time of
submitting the bid and whether the same have taken into consideration or not in the quotations.In the event
of delay delivery and/or unsatisfactory manufacturing progress and supply, the SGPGIMS has the right to
cancel the purchase order as whole or in part without liability for cancellation charges.
In the event of rejection of non-confirming goods the vendor shall be allowed, without any extension of
delivery time to correct the non-conformities, should however the vendor fail to do so within stipulated time,
the SGPGIMS may cancel the order.
46 No Payment shall be made for rejected material nor would the tenderer be entitled to claim for such items.
47 Rejected items would be removed by the tenderer from the site within two weeks of the date of rejection at
their own cost. In case they are not removed they will be auctioned at the risk and responsibilities of the
suppliers without any further notice.
48 In the case of not honoring the supply order, Sanjay Gandhi Postgraduate Institute of Medical Sciences, will
have the right to impose penalty as deemed fit to resort to make purchase at the suppliers cost and risk may
forfeit his security to make purchase at the suppliers cost and risk.
49 In the case of non-supply of stores within stipulated period, it will be at the discretion of the Sanjay Gandhi
Postgraduate Institute of Medical Sciences to accept delivery with late delivery clause, in case of indigenous
goods @ 1% per week maximum to the extent of 10% and incase of import 0.5% per week maximum to the
extend of 5% of the ordered value for delayed supply.
50 All disputes and question, if any arise between the Institute and the bidder out of or in connection with the
terms and conditions contained herein or as to the construction of application thereof, or the respective rights
and obligations of the parties there under or as to any clause or thing herein contained or by reason of the
supply or failure or refusal to supply any material or as to any other matter in any way relating to these
presents shall be referred to the sole Arbitration, President of the Institute/Chief Secretary of the U.P. Govt. or
his nominee. The decision of the sole arbitrator shall be final and binding upon both parties and subject to
adjudication of Lucknow Court. Place for arbitration shall be at Lucknow (U.P.), India. Venue of such
arbitration proceedings shall be the Institute. Arbitration and conciliation Act 1996 and rules made there
under shall be applied to the proceedings under this clause.
51 Sales-Tax Registration certificate/ Vat registration certificate duly attested copy by a Gazzetted Officer should
alsobeenclosed.Sales Tax, certificate or in absence of this certificate you can attach the copy of VAT
registration and copy of current return submitted along with the affidavit from a notary that the firm has
never been black listed must be attached along with the tender documents failing which the tender will be
rejected.
52 The Manufacturer or their Indian representative will ensure a proper after sales service as per our
requirement from time to time, against the guarantee/warrantee clause as per terms and conditions agreed
under negotiations would be provided at our Institute without fail. Any negligence on this account shall be the
sole responsibility of foreign vendor and the liability for compensation will be fixed by the Institute. An
undertaking from the manufacturer that in the event of change of Indian Agent, the new agent will provide
the CMC on similar terms and conditions or the manufacturer himself undertakes the responsibility of proving
the satisfactory after sales services under such events.
53 The Price Bid of the technically qualified vendor will be opened in the presence of authorized representatives.
The vendor may send their authorized representative during the price bid opening.
54 Comprehensive offer would be finalized before placement of order either on comprehensive or semi / non
comprehensive basis (with or without spare / consumables /accessories including labour charges) up to
expected life span of the equipment by the Institute to the tune of 95%uptime of equipment that CMC will be
effective after expiry of warrantee period.
55 Criteria of selection of product and comparison evaluation of rates
In addition to clause No.03 above the criteria for deciding L1 would be as follow:-
Note: Please Note that each tender should be quoted and sealedSeparately if
more than one tender is submitted failing which the submitted tender will
not be received & considered for opening of the same and liable to be
rejected.
Must read before quoting the tender (Mandatory)
The equipments/ items not manufactured in India must be quoted in foreign currency only
and the Institute would establish the letter of credit.
(a) The evaluation report of technical committee will be the final decision for selecting the firm. (b) If the product has been quoted in foreign currency in that case the exchange rate prevailing on the date of
last date of submission of tender. (c) While comparing the rates quoted CMC charges will be included in the quoted rates and 15% additional
cost will be added towards freight, insurance, custom duty, clearing etc.
The price ranking will be carried out as under:-
(i) The exchange rate of the last date of submission of bid will be applicable for price ranking. (ii) The prices for optional items will be excluded for ranking purpose i.e.L-1,L-2 etc. (iii) After omitting ‘optional items’ ranking will be determined as under
Total price: - Price with all accessories as per technical specification + CMC Price (with spares)
for five years after warranty.
Date of currency conversion i.e. last date for submission of tender bid & this will be the comparison rate for the offer made in foreign currency of Financial Bid.
Components to be taken in the consideration to the Financial bid comparison (in case of import purchases) (A) Basic cost of the Equipment (CIF Cost upto SGPGI stores including customs duty and all other
clearing charges). (B) Cost of essential / standard accessories (C) Warranty period of 5years, in case the offered rates is less than the required period then the
cost of paid warranty to be loaded with a cost for left out period. (D) Value of CMC (Comprehensive Maintenance Contract) for next 5 year.
A+B+C+D and CIF SGPGI central stores cost will be incorporated with the total cost of goods
along with indigenous, if any.
Name of Part/ consumables / accessories not covered in the warranty period along with their cost be printed with the bid. These rates will be frozen for period of 5 years followed by yearly escalation upto the maximum extent of 10%, if requested.
The supplier is expected to quote their rate on CIF(SGPGI Central Stores) basis with breakup of FOB (which is to be paid in foreign currency (freight cost, Customs Duty, clearance of consignment, AII Charges & freight uptoLucknow SGPGIMS central stores etc payable in Indian currency. Claim bill for INR shall be initiated on as per actual (documentary evidence) or tendered rate which ever is
lesser.
56 The supplier will get the equipment/consignment cleared from the customs. The customs Duty and clearance
charges as well as freight charges will be borne by the manufacturer/Indian representative as the time of
clearance which will be reimbursed by the Institute on production of documentary evidence. Also the
insurance will be arranged by the firm effective form port of shipment to Central Stores, SGPGIMS, Lucknow
and the charges will be reimbursed by the Institute based on documentary evidence.
JOINT DIRECTOR (MM)
For DIRECTOR Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow
ADULT AIRWAY MANAGEMENT TRAINER INTUBATION MANIKIN
PGI/MM/CCM/15-16/03 01
MANNEQUIN FOR CENTRAL VENOUS CATHETERIZATION FOR INTERNAL JUGULAR AND SUBCLAVIAN VEIN WITH ULTRASOUND GUIDANCE
PGI/MM/CCM/15-16/04 01
STERNAM SAW PGI/MM/CVTS/15-16/03 02
BABY MANIKIN (NEONATAL) WITH INTUBATION HEAD
PGI/MM/NEO/15-16/01 01
FIBEROPTIC PHOTOTHERAPY UNIT PGI/MM/NEO/15-16/02 02
CR CASSETTES COMPATIBLE WITH EXISTING FUJI CR
PGI/MM/RAD/15-16/01 01
BLOOD BANK REFRIGERATOR (50-70 BAGS CAPACITY WITH WIRELESS DATA LOGGER
PGI/MM/TM/15-16/01 10
Blood Bank Refrigerator
Set temperature 4°C.
Temperature range 2°C to 6°C and adjustable with setting accuracy of ±0.1°C.
Capacity: 50 to 70 standard blood bags
Vertical Cabinet (upright) with front door.
Polyurethane Insulation
Microprocessor based temperature controller with integrated audio visual temperature and power alarm
function with digital monitoring display.
User Parameter settings: set point, high alarm point, low alarm point, buzzer off time
Minimum 4 hours battery back up for temperature /power alarm.
Seven days graphic temperature recorder with range of -10°C to +20°C
Door opening audio and visual display alarm.
Should have provision for controlled air circulation for constant temperature distribution.
Stainless steel material for interior walls and shelves, perforated on the bottom for perfect and homogeneous
distribution of cold air.
Air cooled compressor with CFC free refrigerant
Controlled fan cooling system for constant internal uniform temperature distribution at ambient temperature
of 43°C.
Audio and visual alarm for variation in temperature
Interior lighting
It should be operational on 220 to 240 volts at 50 Hz, 3-phase AC
A line voltage corrector of appropriate rating will form part of standard configuration.
The equipment should be compatible with wireless data logging system and data loggers should be supplied
with each equipment with facility for remote monitoring of temperature.
All consumables such as thermographs and batteries should be supplied throughout the warranty period free of cost. REFRIGERATED CENTRIFUGE FOR COMPONENT SEPARATION
PGI/MM/TM/15-16/02 01
Refrigerated Centrifuge
For separation of blood components like packed cells, platelet rich plasma, platelet concentrate, plasma
Microprocessor controlled system to make operation automatic.
Programmable memory: Memory with tamper proof facility.
Stainless steel chamber: Easy to clean, corrosion resistant with provision of both drain and condensed water
collection container.
CFC free refrigerant
Swing bucket blood bank rotor: With metal buckets, 6 x 1000 ml., wind-shielded. Suitable adapters for 12
blood bags of 350 ml. & 450 ml.
Removable plastic cups to hold single/ double/triple/quadruple blood bags.
Insert with hook adapter to spin buffy coat or small volume of blood and balancing weights for inserts
Equipped with automatic lid lock
Centrifugal force: Minimum ceiling - 5000 g.
Speed variation: Microprocessor controlled rotor speed to within 10 rpm of set value. Acceleration and
deceleration profiles shall be available.
Temperature range: -100C to +400C
Microprocessor controlled rotor temperature within 10C of set temperature regardless of the centrifuge
speed.
Programmable time: 0 - 99 minutes with minimum resolution of 1 minute.
Digital display of temperature, speed and time. Minimum no. Of 3 digit resolution. .
Motor imbalance detection: Automatic shut down of centrifuge if rotor load is out of balance with
appropriate indicator. Should incorporate alarms for imbalance detection lid interlock, over temperature,
rotor overspeed
Power requirement: 220/240 volts, 50 Hz. Single phase AC supply.
The equipment shall be suitable for operation from 0 to 400C at 90% Relative humidity. Electronic circuitry
shall be tropicalized for this ambient condition.
Electrical safety conforms to standards for electrical safety IEC-60601/IS-13450
The equipment shall have lockable castors.
Protection of data: In event of power interruption or complete failure data should remain stored
Should have a port to attach with Hospital Computer Information System
It shall have a security lock to prevent unintentional switch off and also unauthorised opening of the
equipment.
Automatic Line voltage corrector/Voltage Stabilizer: A line voltage corrector of appropriate rating should
form part of standard configuration. Copper wound single phase automatic line voltage corrector conforming
to IS: 9815(Pt.I)/94 with latest amendments or equivalent international standards fitted with a voltmeter and
switch to indicate output/input voltage as under:
Capacity/rating: 10 KVA: As per the requirement of the equipment. Input voltage: 140 to 280 volts, 50 cycles.
Output voltage: 220 volts ± 10% volts. Input-out voltmeter and amperemeter. Protection: high-low voltage
cut-off, overload and short circuit protection. The equipment should be supplied with 2 meter cord at input
and fitted with plugs of appropriate rating (15Amp.). Make of the line voltage corrector shall be indicated
MULTI-HEAD TUBE SEALER (BENCH TOP) PGI/MM/TM/15-16/03 01
Multi-Head Tube Sealer (Bench Top)
Should have minimum 5fixed sealing heads capable of making segments of blood bag tubes.
Should also have option for individual seal or multiple seals as required.
Heavy duty radio frequency sealer, US –FDA approved
Automatic detection of the tube by pressing of a lever which activates sensor
Minimum sealing time
No warm up time for the equipment before sealing
Should have separable rupture line to separate tube ends after sealing.
Alarm in case of seal not safe and completed.
Switch mode power supply for uniform sealing irrespective of power supply variations
Compatible with the tubes of various manufacturers of blood bag. Should seals 3.0 to 5 mm tubes with wall
thickness of 0.75 mm.
Indications for Ready, Seal and Power.
Protection against electric shock
To be operational on 220 to 240 V at 50 Hz, single phase
BLOOD BAGS DISINFECTION SYSTEM (AUTOCLAVE) PGI/MM/TM/15-16/04 01
Blood Bag Disinfection System (Autoclave)
Automated, microprocessor controlled operation
Capacity ≥ 100 liters
Should include vacuum cycle, rapid vacuum cycle and non-vacuum cycle with or without drying
Vacuum cycle for steam penetration test
Touch sensitive control panel
Vertical sliding door with front loading and a rectangular stainless steel chamber
Multi-program model allowing at least 5 programs to be stored
To be supplied with load probe and printer
10 year pressure vessel integrity warranty
Delayed start facility
Audible and visible alarms including cycle fault and interruption, sterilization failure, low water level and
door unlocked.
Should comply with standard European (CE) or American (ETL) electrical safety standards.
Should work on 200-250 Volts at 50 Hz
Should have a communication interface for data transfer to a central data capture system.
For indigenous items: should comply with BIS standards
PLASMA THAWING SYSTEM PGI/MM/TM/15-16/05 01
Plasma Thawing Water / Dry Bath
For thawing of plasma at 37oC
Should be US-FDA / CE approved
Should be able to thaw at least 4 units of plasma simultaneously.
Microprocessor based precise temperature control
High performance 1.5 kw heater & compressor to achieve the set temp
Over temperature safety limit, audio visual alarm
LED monitor to display the working status of thawing bath
Continuous water circulation for temp uniformity & rapid thawing
Optical and acoustic signal after heating duration is complete
Should have transparent cover so that plasma bags are visible during thawing process
Integrated leak control
Corrosion –resistant material for construction of body
Round corners for easy wipe disinfection
Full surface dry temperature regulation
Optical and acoustic signal after heating duration is complete
DIELECTRIC TUBE SEALER (BENCH MODEL) PGI/MM/TM/15-16/06 02
Dielectric Tube Sealer (Bench Model)
Heavy duty radio frequency sealer, US –FDA / CE approved
Automatic detection of the tube by pressing of a lever which activates sensor
Minimum sealing time
No warm up time for the equipment before sealing
Should have separable rupture line to separate tube ends after sealing.
Alarm in case of seal not safe and completed.
Switch mode power supply for uniform sealing irrespective of power supply variations
Compatible with the tubes of various manufacturers of blood bag. Should seals 3.0 to 5 mm tubes with wall
thickness of 0.75 mm.
Indications for Ready, Seal and Power.
Protection against electric shock
To be operational on 220 to 240 V at 50 Hz, single phase
AUTOMATED SYSTEM FOR DETECTION OF BACTERIA IN BLOOD COMPONENTS
PGI/MM/TM/15-16/07 01
Automated Bacteria Detection system
Fully automated system capable of detecting bacterial contamination of blood and components
System should be approved by competent authorities such as FDA for use in blood bank
System should work on the reliable colorimetric principle of detection based on CO2 sensor to indicate
growth of organisms.
Every loading position for culture bottle should have its own optics and detection device
System should have built in calibration check
System should be capable of exporting data to external drive for long term storage
System should have facility of analyzing delayed entry specimens with the routine bottles
System should have a efficient capability for bacterial detection in blood components such as continuous
monitoring of samples for growth of organism and continuous agitation.
System should be for minimum of 60 positions.
System should have different type of culture bottles for different applications
System should also be capable for detecting yeast and other fastidious organisms.
System should be provided with printer and ups and should be able to display growth kinetics on the screen.
System should be modular and upgradeable for future requirements.
System should support use of plastic bottles for safety and ease of disposal
System should have FDA clearance for microbial quality control testing in blood banks
STERILE CONNECTING DEVICE PGI/MM/TM/15-16/08 02
Sterile Connecting Device
Should accommodate and weld all types of blood bag tubing in use in our country.
The welding should be seamless.
Should be capable of joining wet-wet/wet-Dry/ Dry-Dry tubes.
Welding should not affect the quality of the tube in terms of its physical and chemical properties and it should
not cause hemolysis.
It should have LED indicators to display the actual status of the ongoing procedural steps and audio-visual
alarm system for any functional irregularities.
The welding accessories should be available with the local agent throughout year.
Compatible UPS with half an hour backup.
Power supply 220V, 50 Hz AC.
BLOOD BAG TUBE STRIPPER PGI/MM/TM/15-16/09 10
Tube stripper
Should be made of sturdy material, rust free
Should have rollers for stripping of tubing
PGI/MM/NEPH/15-16/01 LARYNGOSCOPE 04
SPECIFICATION
LARYNGOSOPE-ADULT (4 BLADE SET) LARYNGOSOPE-PEDIATRIC (2 BLADE SET)
PGI/MM/NEPH/15-16/02 ELECTRONIC DIGITAL BP MEASUREMENT WITHOXYGEN PROBE SPO2 ON STAND
30
PGI/MM/NEPH/15-16/03 MULTIPARA MONITOR 04
6-CHANNEL ICU MONITOR
Specifications:-
Large colored, high definition (800 x 480) TFT touch screen (size more than 12”)
Parameters: SPO2, ECG, NIBP, 2 IBP, TEMP with at-least two pairs of spare leads for each, suitable for adult,
pediatric and neonatal patients each.
More than 72 hours graphic and tabular trends of all parameters.
Facility for arrhythmia analysis.
Drug dose and hemodynamic calculations.
500 measurement data can be stored and recalled
Built-in rechargeable Lithium battery with back-up time of at-least 1 hour.
Equipped with internal printer.
Should be equipped with visual and audible alarm system
Wall mount accessories.
Facility for up-gradation to central monitoring system.
Product should be FDA approved.
Guarantee, warranty, comprehensive maintenance and non-comprehensive maintenance clauses as per the Institute Norms. PGI/MM/NEPH/15-16/04 DISSECTING MICROSCOPE 01
Digital Dissecting microscope with built-in digital camera,
High end zoom digital dissecting microscope offers continuous magnification from 10x - 40x. Eyepiece lenses can be switched out to increase or decrease
this range. Available are 5x, 10x, 15x or 20x pairs.
Auxiliary lenses can be added to the objective lens to modify the magnification at the camera and the binocular eyetubes. Available 0.5x, 0.75x,
and 1.5x auxiliary lenses.
Built-in 2.0 mega pixel digital camera built into microscope.
Includes software.
12 volt 10 watt halogen top and bottom illuminators.
Objective Lenses: 1x - 4x objectives provide a zoom range from 10x - 40x when using 10x eyepieces.
Eyepieces: paired widefield 10x eyepieces, all are 45° inclined, with dual diopter adjustments, interpupillary adjustment from 55mm to 75mm.
Total Magnification: Continuous zoom range of 10x - 40x
Specimen Stage: Large 165mm wide x 220mm deep stage surface. Includes two 80mm stage plates (frosted glass and reversible black/white plastic contrast plates),
blue filter for transmitted light and locked on stage clips.
Stand: Mounted on an all-metal heavy duty post stand, microscope head extends to 17" for higher objects.
Focusing: Large dual focusing knobs with slip clutch to prevent damage to mechanism. Tension adjustment eliminates focus “drift”.
Illumination: Top light is 12v 15 watt halogen, bi-pin with directional beam and rheostat control. Bottom light is 12V 10 watt halogen, bi-pin. Lights operate together or
independently.
Size & Weight: 13" high, extends to 17" for taller objects, 11.2 lbs.
Warranty: Lifetime limited warranty. Camera has a 1-year warranty. Software has 90-day warranty.
Includes: Software, calibration slide, USB cable, vinyl dust cover and owner's manual.
CAMERA SPECIFICATIONS:
3.0 mega pixel camera built into microscope.
1/3" CMOS Imaging Device.
Minimum Illumination - 3 LUX
Connects to computer via USB 2.0 Port - self-powered through computer.
Captures moving images at 10-20 frames per second.
Effective pixels 2048 x 1536.
Images can be captured and saved as either .jpg, .bmp or .mig files.
SYSTEM REQUIREMENTS :
Windows XP or above
Intel Pentium
CPU 2 Ghz or above
RAM 1 GB or above
Hard Disk 500 MB or above
Video card 128 MB or above
CD-ROM drive
USB 2.0 port
PGI/MM/NEPH/15-16/05 AUTOMATED ELECTRONIC ADJUSTABLE SPACER PIPET 04
1- Single Channels Electronic Pipettes
1. Fast navigation (Quick, easy controls simplify)
2. Versatile range of pipetting modes for any task.
3. Save time-store your favorite protocols.
4. Secure service data, lockable modes, and password.
5. Configure the pipette for simplicity and security.
Volume Range
1. Single Channels Electronic Pipette 0.5 μl – 10 μl
2. Single Channels Electronic Pipette 2.0 μl – 20 μl
3. Single Channels Electronic Pipette 10 μl – 100 μl
4. Single Channels Electronic Pipette 20 μl – 200 μl
5. Single Channels Electronic Pipette100 μl – 1000 μl
2- Multichannels (8 Channel)Electronic Pipettes
1. Superior channel-to-channel consistency
2. Simplify repetitive microplate pipetting
3. Lightweight, yet balanced and robust.
4. Lightest Touch
5. PureSpeed funtionality is installed in all type of tips.
Volume Range
1. Multichannels (8 Channel)Electronic Pipette 1.0 μl – 10 μl
2. Multichannels (8 Channel)Electronic Pipette 2.0 μl – 20 μl
3. Multichannels (8 Channel)Electronic Pipette 5.0 μl – 50 μl
4. Multichannels (8 Channel)Electronic Pipette 20 μl – 200 μl
5. Multichannels (8 Channel)Electronic Pipette 100 μl – 1200 μl
3- Multichannels (12 Channel)Electronic Pipettes
1. Superior channel-to-channel consistency
2. Simplify repetitive microplate pipetting
3. Lightweight, yet balanced and robust.
4. Lightest Touch
5. PureSpeed funtionality is installed in all type of tips.
Volume Range
1. Multichannels (12 Channel)Electronic Pipette 1.0 μl – 10 μl
2. Multichannels (12 Channel)Electronic Pipette 2.0 μl – 20 μl
3. Multichannels (12 Channel)Electronic Pipette 5.0 μl – 50 μl
4. Multichannels (12 Channel)Electronic Pipette 20 μl – 200 μl
5. Multichannels (12 Channel)Electronic Pipette 100 μl – 1200 μl
4-Electronic Pipetting Accessories
1. Charging stand Recharge in less than an hour. 2. Wall power supply Chargeable while between work. 3. Filters Prevent liquids and aerosols entering the shaft. 4. Reservoirs Sterile polypropylene reagent reservoirs. 5. Reader and software( Manage assets, help improve regulatory compliance )
RE-TENDER
PGI/MM/PM/14-15/02 ENDOBRANCHIAL CRYO AND ARGON
PLASMA COAGULATION SYSTEM
01
A1: Essential supplies with functions and specifications
Cryo-Unit satisfying these criteria
1. Operating Pressure Range: 40 - 60 bar. 2. Coolant: N2O or CO2. 3. Gas Consumption for freezing: ca.35 g – 50 g/min. 4. Gas Consumption for defrosting: ca.3 g. 5. Max.exhaust gas volume: 40 – 60 l/min. 6. The Unit should have Manometer to monitor operating pressure. 7. It should have different indicator lamp to indicate freezing and defrosting phase. 8. It should be provided with connection pipe for gas exhaust. 9. It should be mounted in a cart with cylinder case for easy mobilization. 10. Cryo system activation should be via footswitch (Explosion protected) & minimum
freezing temperature should reach within 5seconds. 11. It should have wire basket, gas hose (flexible with length 0.7-1m), gas filter for N2O or
CO2, filter cartridges (5Nos), cylinder connection with pin-index code (as applicable in India) and gas bottle adapter
12. It should have cylinder cover for N2O cylinders with international standard 13. It should have sterilization box (both small and large) for cryo-probes 14. One extra-cylinder for cryo gas (with local N2O or CO2gas prefilled) be supplied along
with the main equipment 15. All Cryo probes and accessories should be autoclavable. 16. The unit should be in compliance with type BF
A-2: Essential accessories with functions and specifications
All probes with connectors for use with flexible bronchoscope and rigid bronchoscope with sizes
ranging from 1.9 mm to 2.4 mm and length 780 mm to 1050 should be supplied along with the
main equipment
Flexible Probe with 2.4mm diameter, length 780mm (5 Nos)
Flexible Probe with 2.4mm diameter, length 900 mm (5 Nos)
Flexible Probe with1.9mm diameter, length 780mm (5 Nos)
Flexible Probe with1.9mm diameter, length 900mm (5 Nos)
Flexible Probe with1.9mm diameter, length 1050 mm (5 Nos)
Rigid bronchoscopy probe with 3mm diameter, length 530mm (5 Nos)
Connecting adapter for flexible and rigid probes
All necessary cryo tip used with bronchoscopes
C: General specifications for the system as a whole
1. All metallic instruments and accessories should be autoclavable 2. Shall meet standard environmental and safety parameters 3. Should be FDA, EUROPEN CE or UL approved product 4. Warranty for five years 5. CMC for five years after expiry of warranty
SPECI
FICATI
ONS
OF
CRYO
UNIT
WITH
FLEXIBLE PROBES, RIGID PROBES AND BIOPSY PROBES
SPECIFICATIONS OF ARGON PLASMA COAGULATION UNIT WITH ELECTROCAUTERY FACILITY
A1: Essential supplies with functions and specifications
Electrosurgery unit with Argon Plasma Coagulation satisfying these criteria
1. Microprocessor controlled Electrosurgery unit with Argon Plasma Coagulation unit 2. Should have Bipolar CUT/COAG facility 3. Should have AutoStart and AutoStop facility for Bipolar modes 4. Facility to store up to 98 programs 5. Should have TFT Display 6. Should have visual indicator for the actual power being used 7. Should have special Micro-bipolar CUT/COAG modes (1-50w) 8. Should have ENDO Cut Mode 9. Should have three different APC modes suitable for different indications
Precise APC – adjustment made using the effect settings
Pulsed APC – adjustment made using the parameter power settings
Forced APC – adjustment made using the parameter power settings 10. Adjustable argon flow rates and automatic monitoring of argon supply 11. Visual and audible indicator for Argon Cylinder content 12. Should be supplied with flexible argon beam applicators for straight firing, side firing and
circumferential firing for argon beam-5 Nos. each. 13. Power should not more than 200Watt. 14. Unit should be upgradable with water-jet for EMR/ESD
A-2: Essential accessories with functions and specifications
Argon cylinder with Argon gas (99.99% & higher degree of purity) (2 Nos)
Trolley for the whole equipment
Flexible bronchoscopy probe with filter integrated for APC (2.3 diameter, length atleast 2.2
m {5 Nos})
Rigid bronchoscopy probe with filter integrated for APC (5 Nos)
Pressure reducer with sensor
Pedal foot switch
Connecting adapter for flexible and rigid probes
All necessary accessories used with bronchoscopes
C: General specifications for the system as a whole
6. All metallic instruments and accessories should be autoclavable 7. Shall meet standard environmental and safety parameters 8. Should be FDA, EUROPEN CE or UL approved product 9. Warranty for five years 10. CMC for five years after expiry of warranty
NEW TENDER
PGI/MM/PS/15-16/01 URODYNAMIC MACHINE 01
Specifications of Urodynamics equipment
Should be able to perform following studies with the machine:
- Filling Cystometry
- Voiding Cystometry (Pressure- Flow studies)
- UPP (Urethral Pressure Profiles, Rest & Stress
- EMG (Electromyography) - wireless
- Automatic Leak Detection
- Video-urodynamics
- Anorectal Motility Studies
- Biofeedback ( paediatric)
Flow sensor – wired, specifically designed & sensitive for low flow-rates (ie paediatric flow).
Puller - To allow urethral pressure profile studies. Control from software (start/stop & adjustable speed).
EMG (wireless) - Separate module, connects to main
system input via USB extension cable. Vaginal and rectal probes should be available. ‘Full Wave’ or
‘Envelope’ signal.
1 EMG Channel
2 electrodes, 1 reference electrode.
Patient input protection: ~6kOhms
Input range: 1mV full scale
Input resolution: >100nV (averaged)
Acceptable DC voltage: 600mV maximum
Input impedance: 1010 ohms // 1pF
Input impedance imbalance: >40%
Common mode rejection: >100dB.
Bandwidth: 10Hz~1000Hz
Optional Notch: 50Hz
Input referred noise level: 2μV (averaged)
Infusion pump – 3 roller peristaltic fillng pump. Software control (start/stop & speed selection).
Remote Control – Hand-held remote control to allow system operator to control SmartDyn urodynamics
system without having to touch the PC/mouse
Functions
Recording start/stop
Pump start/stop
Puller start/stop
Video clip start/stop
Record video snapshot
Zero channels
5 additional buttons (1-5) that can be programmed by the use
Urodynamics Kit – Pressure transducers for urodynamic testing. Colour coded labels and cables (Vesical,
Adbominal and Urethral channels). Auto 100mmHg test / calibration button. Fitted to bracket/clamp.
Technical data
Method: Water filled
Sensitivity: 5.0 Nominal uV/V/mm Hg
Range: -50 – 350mmHg
Reusable transducer (to be used dome).
Micturition Chair – Height adjustable, folding arms, detachable seat and cover, removable funnel.
Micturition stand – voiding studies, height adjustable, removable funnel.
Automatic Leak Detector – detects leaks during procedure and software automatically marks trace with a
‘Leak’ event.
Technical data
Detection method: Temperature
Number of detections: Unlimited
Compatible catheters: 6Fr
PC, Monitor, Printer – latest specification, options available, Laptop or Desktop
Pressure Transducers for use with air-charged catheters. Technical Data
Method: Air-charged
Connector: Lemo 18 pin
Sensitivity: 5.0 Nominal uV/V/mm Hg
Drift: <1.5 mmHg over 4 Hrs
Software characteristics: Windows platform, multi-language.
Standards and terminology as according the the ICS (International Continente Society)
Nomograms, ICS, Pediatric, Siroky, Abrams-Griffiths, Werner Shaffer, Pressure-Flow loop,
Pressure v Volume, Compliance.
Connectivity to Hospital information system and PACS DICOM work-list & DICOM Storage
Rehabilitation software – Biofeedback for paediatric usage, using surface, needle or plug electrodes.
Procedure setup – user configurable procedures, traces, colours, layout etc.
Event markers – user configurable toolbars, and event markers (icons and/or text)
Archiving capabilities – possibilities to export/import datafiles to other PC’s
Accessories Double Lumen catheter 6 Fr 25 Nos. Rectal Catheter 4Fr with flap 25 Nos Pump Tubeing 25 Nos. EMG Electrode 25 Nos. Ano Rectal Manometry catheter 3 channel
OPTIONAL
Video urodynamics – allows x-ray images to be combined with the urodynamics traces.
Display/record/print options all available within SmartDyn software. X-ray system is connected to
SmartDyn via an adapter cable.
Technical data
Composite video input (RCA/Phono) PAL, SECAM, NTSC
S-Video input (mini-DIN) PAL, SECAM, NTSC Adapter cable (BNC to RCA)
On site technical demonstration in the department is essential.
PGI/MM/PS/15-16/02 SURGICAL INSTRUMENTS 01 Set
SPECIFICATIONS FOR ROUTINE SURGICAL INSTRUMENTS
Sl. no Instrument Specifications
Scissors
1 Stevens tenotomy scissors Tapering, fine, tip. Curved.
12.5 cms, 5”
2. Reynolds’ scissors Fine, pointed
145 mm
175 mm
3. Metzenbaum curved scissors Tungten carbide cutting edge, gold plated rings
14.5cms. Curved
16 cms, curved
18 cms, curved
20 cms curved
23 cms, curved
4 Metzenbaum straight scissors 16cm
18 cm
20 cm
5. Potts scissors Fine, pointed, curved
180 mm
Dissecting and tissue forceps
6 Mc. Indoe toothed tissue holding forceps
Delicate, extremely fine teeth
15cms, 6”
7 Gerald toothed tissue holding forceps
17.5 cms, straight
8 Waugh toothed tissue holding forceps
20 cms, straight
9 Mc. Indoe tissue holding forceps, non toothed
6”, 15 cm
10 Cushing’s tissue holding forceps, non toothed.
18 cms, serrated tips, non-toothed
20 cms
25 cms
11 DeBakey’s atraumatic vascular forceps
Vascular forceps, atraumatic jaws, 1.0 mm wide tip
15 cm
19.5 cm
24 cm
12 Micro tissue forceps Round handles, soft spring tension, platform tip, straight.
15 cms. Straight tip
21 cms. Straight tip
Needle holders
13 Needle holder-Crile Wood Delicate pattern
15 cms
14 Jameson needle holder 23 cms
15 De Bakey’s needle holder Tungsten –carbide inserts, gold plated ring handles, slender pattern
18 cms
23 cms
25cms
16 Ryder (very delicate,suture size 5/0 &smaller)
1 mm jaw, diamond dust coating /tungsten carbide inserts on the inside of jaws, gold plated ring handles, serrated jaws
14 cms,
18 cms,
22 cms,
25 cms
17 Castroviejo needle holder Straight, diamond dust coating/tungsten carbide inserts on the inside of jaws, gold plated ends
14.5 cms
18.0 cms
18 Micro-needle holder Round handle, straight tip, with ratchet, diamond dust coating/tungsten carbide inserts on the inside of jaws.
23 cm
Vascular clamps, hemostatic forceps, vessel clips
19 Bull dog clamp-Dieffenbach Curved
38 mm total length,12 mm length of jaw serrations
48 mm total length, 16 mm length of jaw serrations
20 Bull dog clamp, Diethrich Curved, 48 mm total length, 10 mm length of jaw serrations
21 Mini Bull dog clamp CVD 35mm CVD 35mm
22 Mini Bull Dog Clamp CVD 45 mm CVD 45 mm
23 Bull dog clamp-De Bakey Curved
78 mm, 18 mm length of jaw serrations
86mm, 26 mm length of jaw serrations
24 Cooley vascular clamp(coarctation ,patent ductus clamp)
Gentle curve of the jaw,
Total length : 18cms
Length of serrated jaws:63mm
25 Debakeys vascular clamp
( patent ductus clamp)
Gentle curve of the jaw
Total length: 20 cms
Length of serrated jaws: 92.5 mm
26 Cooley vascular anastomosis clamp (single angle curve of jaw)
16.5 cms length, 30 degree jaw angle
27 Cooley vascular clamp (ring handle bull dog clamp)
Double angled curved jaw, length 11.5 cms
28 Baby-Satinsky vascular anastomosis clamp
Double angle curve jaw,
length 150mm
29 Cooley vascular anastomosis clamp (double angle curve jaw)
double angle curved atraumatic jaws,
Length 16 cms,
jaw width: 24 mm
30 Cooley vascular anastomosis clamp Double angle curved jaw, Length: 17.5 cms,
jaw width: 20mm
31 De- Bakey –Satinsky tangential occlusion clamp
Double angle curved jaw
Total length: 23.5 cms
Jaw length: 68 mm
Width of jaw: 32mm
32 DeBakey tangential occlusion vascular clamp (double angle curve jaws)
Total Length 22 cms,
jaw width 38mm
33 DeBakeys dissecting & ligature forceps, profunda clamps
Atraumatic jaws, smooth rounded curve.
Total length 19 cms
Length of serrated jaws: 77 mm
34 Debakey pediatric vascular clamp Small, 45 degree, 9.8 cms, jaw length 15 mm
Medium, 45 degree angle, 10.5 cms, jaw
length 30 mm.
45 degree angle, 11.9 cms, jaw length 40 mm
35 Wirthlin splenorenal shunt clamp 16.5 cms long, “Atraugrip” jaw, 3.5 cms, spring handle, 1X6 ratchets
36 Stoney splenorenal shunt clamp 23 cms. long, extrafine atraumatic jaw 2.5 cms, spring handle, 1X9 ratchets
37 Artery c lip-Micro Hartmann
Very delicate pattern
9 cm-straight
9 cm-curved
38 Micro-Halstead-mosquito 12.5 cms. Straight
12.5 cms. curved
39 Roberts artery forceps 22.5 cm-curved
40 Crafoord artery forceps 24.5 cm-light curved
Dissecting and ligature forceps
41 Mixter right angle dissecting & ligature forceps
Right angle dissecting and clamping forceps, very delicate jaws with longitudinal serrations, cross serrated tips
18 cms
22 cms
25 cms
42 Lahey dissecting & ligature Forceps Fully curved jaws with longitudinal serrations
20 cm
23 cm
43 Micro-Adson dissecting &ligature forceps
14 cms.
44 Gemini dissecting & ligature forceps
13 mm
18 mm
20 mm
23 mm
28mm
Tissue holding clamps, sponge holding forceps, towel clips
45 Desjardins gall duct & cystic forceps
22 cms
46 DeBakey atraumatic Intestinal & tissue holding forceps
Intestinal & tissue holding forceps , jaws with atraumatic serrations
Jaws 20 mm wide, 25 cms
47 Backhaus Towel clamp 8.0 cms
11 cms
48 “Simplex” tubing clamp 12 mm width
49 GROSS” dressing and sponge forceps with catch
Atraumatic, serrated jaws with slender oval fenestration, with catch
14.5 cms, curved
18 cms, curved
49 “Foerster-ballenger” Sponge holding forceps
Small loop jaws, serrated
18 cms-straight
24.5 cms-curved
50 Baby Allis 13 cms length, 4x5 teeth
51 Boys-Allis 15.5 cms length, 5x6 teeth
52 Allis 19 cms length
53 Babcock organ & tissue holding forceps
15.5 cms. Length
20 cms length
54 Baby Kochers atraumatic intestinal clamp
Curved,13 cms length
55 Kochers atraumatic intestinal clamps
Curved, 21 cms
56 Blake gall stone holding forceps Curved, 20.5 cms
Retractors
57 Kocher-Langenback retractor Blade:6 mm wide-25 mm deep
Blade: 11 mm wide-41 mm deep
Blade: 15 mm wide-35 mm deep
58 Masing vein retractor Blade 6x12 mm, length 14 cms
59 Cushing Vein retractor Length 17.5 cms, blade 10X10 mm
60 Nerve and tendon hook 16 cms length, 7 mm wide, semi-circular curved blunt tip
61 Adson dura and nerve hook Right angled end, blunt tip
Length: 19 cms, blunt tip
62 Malleable retractors (Stomach & intestinal spatulas)
Ribbon retractors, malleable, stainless steel
12 mm width, 20 cms length
Ochsner ribbon retractors, malleable, stainless steel
30 mm width, 33 cms. length
50 mm width, 33 cms. length
75 mm width, 33 cms.length
63 Volkmann hand retractors 2 prongs,semi-sharp, blade: 8.5x8 mm
3 prongs, semi-sharp, blade 8.5x 13 mm
4 prongs,semi-sharp, blade 8.5x19 mm
64 Harrington retractor Blades:123x45 mm
Blades: 123x64 mm
65 Allison lung spatula 40 mm blade width, 255 mm length
54 mm blade width, 320 mm length
66 Morris retractor Total length: 24.5 cms
Blade: 70 x 50 mm
Blade: 70 x 65
67 Doyen retractors for deep pelvic surgery
Length 24 cms
Blades:35 mm wide, 90 mm deep
Blade:45 mm wide, 120 mm deep
Blade:60 mm wide, 160 mm deep
68 Doyen bladder retractor Length: 25 cms
Blade:53mm depthx80mm width
69 Daever retractors Standard pattern, flexible
18 cms. long, 19 mm wide
23 cms long, 25 mm wide
30 cms long, 38 mm wide
70 “MIKULICZ” abdominal retractors for deep abdominal surgery , 26 cms
Blade:35 mm wide x 91 mm deep, length: 24 cms
Blade:55 mm widex 86 mm deep, length: 25.5 cms
Blade:50 mm widex 121 mm deep, length: 25.0cm
71 St. Marks pelvic retractor Blade: 174x60mm, length: 330mm
72 Rochard table mounted self retaining abdominal retractor
Mounted frame for fastening to the lateral bars (both sides)of the operating table
Blade sizes: 48 x 90mm
48 x 120mm
73 Weitlaner self retaining retractor Standard pattern with prongs
Length 11 cms, semi-sharp prongs
Length 13 cms, semi-sharp prongs
Length 16.5 cms, semi-sharp prongs
74 Balfour –baby self retaining abdominal retractor
Lateral blades: 27mm deep, central blade: 21 x 24 mm
75 Balfour self retaining abdominal retractor
Lateral blade: 60mm deep, central blade:47 x 80mm
Lateral blade: 60 mm deep, central blade: 80 x 80 mm
76 Denis Browne self retaining retractor
Frame: 1 infant size, 1 pediatric size (175 x 150 mm)
4 blades: 40 x 30 mm
4 blades : 20 x 30 mm
77 Finechietto rib retractor Shaft length: 95mm, blades:18 x 21
Shaft length:180 mm,blades:28 x 32
Shaft length:200mm, blades:36x45
Shaft length: 260mm, blades:65 x 65
78 Table mounted self retaining abdominal retractor system
For infants & smaller children
For older children & adolescents
Table mounted self retaining retractor system with assorted types and sizes of retractors (Retractors: Richardson, Kelly, malleable, baby Harrington, Daever etc.)
79 Benson’s pyloric muscle spreader Length: 155 mm
Rectal surgery instruments
80 Killian rectal speculum for children Length 145 mm, blade 70 mm x 7 mm
81 Sims rectal speculum for children Length 19cm, blade 60 x 20 mm
82 Parks rectal spreader Consisting of spreader, 2 lateral blades, one central blade with cold light carrier.
Lateral blades: 70mm deep
83 St. Marks, Modif. Girona perineal spreader
Perineal spreader
84 Rectal suction biopsy forceps For taking rectal mucosal & submucosal biopsies in newborns & infants.
Has 3 detachable tips
85 Punch biopsy forceps for rectum Handle 140mm, Shaft 250mm
86 Fistula probes Straight tip
Curved tip, 45 degree angle
87 Uterine Hegar dilator set Diameter ranging from 1 mm-26 mm
Electrosurgical instruments
88 Electrosurgical Metzenbaum dissecting scissors
180 mm length, fine tip
89 Electrosurgical monopolar forceps 130 mm length
200 mm length
90 Electrosurgical bipolar forceps 16 cms length, straight tip 9 mm
Suction instruments
91 Pool sump suction tip Suction canula with outer tube to be screwed off.
Length: 22.5 cms
92 De Bakey suction canula With finger cut off & stylet
Olive diameter: 9 mm
Length: 160mm
93 Adson suction canula With finger cut off &stylet
Olive diameter: 8mm
Tip diameter: 3 mm
Length: 16.5 cm
94 Barron suction canula With finger cut off & stylet,
Tip Diameter:2mm
Length: 16cms
95 Zoellner suction canula Diameter: 2.5 mm
Length: 180mm
Miscellaneous trays and bowls
96 Kidney tray set All sizes
97 Round bowls set All sizes
Dilators
98 Urethral dilator set All sizes
99 Gum elastic bougies for esophageal dilatation
100 Retrograde esophageal dilators:
Tucker silicone (latex free)
retrograde bougies
101 Savary Gillard’s esophageal dilators
Spinal laminectomy instruments
102 Kerrisons bone punch Jaw position 40 degree upwards: 7 inch, 8 inch
Jaw position 90 degree upwards: 7 inch, 8 inch
103 Bone chisel Straight, curved
104 Periosteal elevator
105 Ruskin Rongeurs Straight, curved
106 Lempert Rongeurs Curved
107 Cobb osteotomes Straight, curved
108 Dura hook
109 Nerve root retractor
110 Bone currette
111 Self retaining lamina spreader
112 Laminectomy retractor
Rib resection instruments
113 Langenbeck Periosteal Elevator Sharp, Blunt
114 Coryllos Doyen Rib Raspatory Left, right
115 Alexander Periosteotome
116 Stille Double Action Bone Rongeur Curved
117 Stille Rib Shears
118 Alexander Rongeur Double Action
119 Coryllos Bethune Rib Shears Left, Right
PGI/MM/PS/15-16/03 ARGON PLASMA COAGULATION 01
Specifications for argon beam coagulator with diathermy
Should have facility for argon enhanced coagulation for no contact coagulation over large surface areas and rapid
hemostasis.
Should be able to facilitate cutting with minimum smoke and maximum visibility.
Should have low flow rate to prevent over pressurization in laparoscopic procedure and should be able to
automatically invoke at system startup.
Should have facility for selecting standard flow rate for open procedures.
Should have audio and visual alarms for overpressure condition.
Should be supplied with all necessary accessories for open surgery.
Should have cylinder capacity-indication facility.
Should have option for connecting two cylinders.
Should be supplied with compatible micro –controller based electrosurgical cautery having both monopolar and
bipolar outputs for all surgical procedures.
Should be able to monitor changes in tissue impedance continuously and adjusts power.
Monopolar outputs should have three cutting modes.
It should have three coag. Modes.
It should have three bipolar modes.
It should have pt. Plate monitoring facility and should give audiovisual alarm and deactivate output.
System should have audio-visual alarm facility, to indicate any breakage of direct contact b/w the pt. and patient
plate.
The unit should have two hand switching and two foot switching monopolar outputs and one hand switching and
foot switching bipolar outputs.
The unit should have individual digital display of power for bipolar, monopolar cut and monopolar coag.
System should have separate monopolar and bipolar foot pedal.
The unit should be software upgradable and compatible with ultrasonic surgical aspirator.
Should be mounted on a trolley.
The unit should have RF activation port.
The unit should not have RF leakage current more than 150 ma.
It should have safety standard of UL, CUL, and IEC-601-2-2.
It should be US FDA approved.
PGI/MM/PG/15-16/02 BREATH ANALYZER, HYDROGEN AND METHANE ANALYZER
01
Specification for Breath analyzer; Hydrogen and methane analyzer for pediatric
use
The machine should detect hydrogen & methane in exhaled air.
The analyzer should be simple, specific and accurate by one part per million (1 ppm) for
recording hydrogen & methane gases.
The analyzer should give corrected reading for the hydrogen & methane gases taking account of O2
gases percentage (%).
The moisture driers should be free from heavy metals.
System should have short warm up time, less than 1 hour
On line Breath Sampling for instant results and patient compliance
Humidity levels 30 - 75 % Non-condensing
Should have low calibration requirement frequency
It should be CE certified.
It should have both direct measurement & breath bag measurement possibility
System should have screen displaying real time reading graphs and values
Analyzer should have inbuilt suction system to suck the sample directly from Breath Bag
Consumable should contain Anti-Bacterial Filters for Optimum Infection control
It should be complete with software & consumables such as breath bags - 100 Pcs ,on line mouth
pieces - 100 Pcs ,filters - 5 No..
Latest model is mandatory
Warranty and guarantee as per institute rules
Consumable should be mentioned separately with costing
PGI/MM/PG/15-16/03 STATDIOMETERWITH INTEGRATED WEIGHING SCALE 02
Specification for Stadiometer with integrated weighing scale
There should be only one-piece equipment having stadiometer integrated with weighing scale.
Equipment should be pediatric and adolescent age group friendly and comfortable to subjects
during measurements
LED based display of measurement data with touch screen facility with auto 8MI calculator.
Integrated software machine with Z scores data for height and weight of Indian children ( WHO
standards) will be preferred.
Scaling data for height should also be displayed on the measuring rod and manual measurement
of height should also be available.
Frankfurt line facility for accurate positioning of head during height measurement
Graduation for height should be in millimeter and centimeter with
standard error not more than 1 millimeter.
Instant weight recording with standard error of not more than one gram.
Power supply based equipment with battery back up.
Automatic time bound on/off switch.
Measurement data storage facility with transferable soft copy of data
Comprehensive warranty on all the items is mandatory
Should provide track record of performance at other centers in India.
Latest model
PGI/MM/I.R.F./15-16/01 DEEP FREEZER -24 DEGREE 03
SPECIFICATIONS FOR DEEP FREEZER -24 DEGREE
Designed for easy access and reliable storage.
Capacity: 260 to 300 ltr.
Ambient temp. 32oC
Temperature Range (oC) : 16 oC / -24 oC
5 Sealed drawers, 2 shelves with transparent front, ensure a good overview of samples.
System should have digital display
System should have visual and acoustic alarm
High temperature alarm
Right Hand hinged reversible door
Castors at back
Frost free system
All around sealed drawers to prevent frost escape when opening door.
Power Supply: (V) 230
Frequency (Hz): 50
HCFC/CFC free refrigerant
PGI/MM/BIOSTAT/15-16/01 UPS (20 KVA) 02
PGI/MM/MS/15-16/02 REFRIGERATOR 60
SPECIFICATIONS:-
Fridge Capacity 100 Ltrs. (CFC Free) Single Door.
Firm to mention the type of cooling gas.
Warranty: five years
Comprehensive Annual Maintenance Charges.
Consumables if any not covered under CAMC/Warranty.
PGI/MM/MIS/15-16/01 SERVO VOLTAGE STABILIZER 02
SPECIFICATION FOR SERVO VOLTAGE STABILIZER (200 KVA)
Servo Voltage Stabilizer micro controller digital display consisting of the following specifications:-
Capacity: 200 KVA 3 Phase, 4 Lines
Input Supply: 300-460 Volts
Output Supply:415 ±1%.
Winding: 100% Copper wound
Cooling: Oil cooled
Type: Unbalanced supply and load, suitable for 3 phase 4 lines unbalanced/ balanced supply and
unbalanced load. The unit consists 03 No. single phase individually AC servo motor controlled connected
in star configuration.
PGI/MM/MIS/15-16/02 VOLTAGE STABILIZER 10
PGI/MM/HEMA/15-16/01 CARDIAC TRANSPORT MONITORS WITH ALL ACCESSORIES
10
A. CARDIAC MULTIPARAMETER MONITOR (Middle End Model)
1. The monitor system should be US FDA approved for Quality assurance. 2. The modular monitor should measure Basic Parameters like 3/5 Lead ECG, Resp, Dual Temp, SpO2 for low
perfusion, NIBP & ETC02 3. Should be capable of up gradation to Cardiac Output (CO),4IBP& AGM. Prices for Upgrades should be quoted
separately. 4. The monitor should have highly visible, bright 12.1” color TFT touch screen display for easy viewing from
distance. 5. The monitor should display at least 8 waveform traces on a single screen.
6. The monitor should have flexible display mode for various monitoring requirement. Bigger font of numeric should also be available.
7. There should be provision for using wireless LAN card & fixed compact flash memory card with power off storage function.
8. There should be alarm limit setting for every parameter 9. It should have emergency nurse call alarm function and Defib-Synch function. 10. It should have fanless design. 11. The monitor should be capable to support wireless networking and compatibility to use with Central
Monitoring System (Wireless CMS should be quoted optionally). 12. There should be complete ST segment, Arrhythmia analysis with Pace detection facility. 13. The monitor should have oxyCRG screen& Monitor should have both touch screen and rotary knob for easy
access. 14. It should have drug calculation & titration table. 15. It should come with rechargeable battery with 2 hours of battery back up
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B. CARDIAC MULTIPARAMETER MONITOR (Lower End Model)
1. The monitor system should be US FDA approved for Quality assurance. 2. The monitor should measure Basic Parameters like 3/5 Lead ECG, Resp, Dual Temp, SpO2 for low perfusion,
NIBP & ETCO2 3. Should be capable of up gradation to Cardiac Output (CO) & 2IBP. Prices for Upgrades should be quoted
separately 4. The monitor should have highly visible, bright 12.1” color TFT touch screen display for easy viewing from
distance. 5. The monitor should display at least 8 waveform traces on a single screen 6. The monitor should have flexible display mode for various monitoring requirement. Bigger font of numeric
should also be available. 7. There should be provision for using wireless LAN card & fixed compact flash memory card with power off
storage function. 8. There should be alarm limit setting for every parameter 9. It should have emergency nurse call alarm function and Defib-Synch function. 10. The monitor should be fanless design. 11. The monitor should be capable to support wireless networking and compatibility to use with Central
Monitoring System (Wireless CMS should be quoted optionally). 12. There should be complete ST segment, Arrhythmia analysis with Pace detection facility. 13. The monitor should have oxyCRG screen and monitor should have both touch screen and rotary knob function
for easy access. 14. It should have drug calculation & titration table.
15. It should come with rechargeable battery with 2 hours of battery back up.
PGI/MM/HEMA/15-16/02 DROP (VOLUMETRIC) INFUSION PUMP
15
VOLUMETRIC DROP INFUSION PUMP
Flow rate from 0.1 to 1000 ml/h with increment of 0.1 ml/h in Micro Mode and 1ml/h in Macro Mode,
Accuracy should be +/- 5% with the recommended sets
Volume infused should be displayed continuously
Should offer at least the following setting modes to be adapted to the hospital medical Practice: Rate only, Rate + Volume, Volume / Time, Ramp up / Ramp Down, Primary / secondary, Sequential, Loading dose, Bolus, Micro Mode
Should offer the possibility to calculate automatically the flow rate based on set volume divided by set time
The pump should offer an auto-test able to check the occlusivity of the Pump with its set, to prevent the risk of free flow prior to starting the infusion
Occlusion and Disconnection of the line should be warned at the earliest, (Alarm and Pre Alarm)
Pump should warn of a pressure rise at low flow rate, whatever the pressure limit is
Pump should warn of a pressure drop, whatever the pressure limit is
Pump should have an Occlusion Pressure Pre alarm and alarm
In-line pressure should be indicated in mmHg and graphically,
Pressure limit should be adjustable from 100mmHg to 900mmHg, with increment of 50mmHg or better,
Pressure limit should be adjustable from 100mmHg to 900mmHg, with increment of 50mmHg or better,
Pump should offer an anti Bolus System at occlusion release.
Should be able to detect air in line after the pumping system for a better air ingress detection
Alarms should be indicated by means of sound signal, dedicated alarm light, and written messages
The Pump should preferably have 2 Large Screens (LCD and LED for better control)
Battery life at 125 ml/h should not be less than 4 hrs and remaining battery life should be indicated hrs and min,
The Pump should give the possibility to display the drug name.
Changes in infusion parameters (Flow Rate/ Pressure etc..) should be possible without stopping the pump.
Drop Detector should not be compulsory it should be optional,
Weight less than 3 kg,
Recall of the last parameters at power on is a must
Pump should have an event log capability including at least 500 last dated events,
RS232 Connection should be available.
Nurse call capabilities should be available,
Time of the Preventive Maintenance should be warned by the pump, Time setting should be customized. But Warning should not stop or avoid the pump to operate,
Compliance with CEE 93/42 directive on medical device CE 0459, compliant with CEE 89/336 directive ( electromagnetic compatibility) waterproofed protection against splashing fluids : IP31, protection against leakage current :
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PGI/MM/HEMA/15-16/03 DEFIBRILLATOR 01 BI PHASIC DEFIBRILLATOR MONITOR
1) The machine should have facility for ECG monitoring, Manual Defibrillation (external & internal), AED and transcutaneous external pacing for adult and pediatric use
2) The unit should have facility of synchronized cardioversion 3) It Should have Latest Bi Phasic Technology with Energy Selection from 1 Joule to 200 Jules. 4) It should have at least 5” Colour TFT Display. 5) It should have 5 Lead ECG Display.
6) It Should have Compact Design Weight should be Less Than 10 KG . 7) It Should have Powerful battery Backup (60 Shocks of 200 Jules) on Fully Charge battery 8) It should have fast 9) It should have Shock proof for Transport use. 10) It Should have Thermal Recorder for ECG Recording. 11) It Should have 72 hours of Trend Memory and up to 1000 Event Storage for a Patient. 12) It should have Less Than 5 second for Charging 200 Jules for Quick Shock. 13) It Should have AED &Non invasive pacing (Transcutaneous) with Default configuration Meets 2005 AHA
Guidelines. 14) It Should Record for Marked Events, Charge,Shock and Alarm. 15) It Should have inbuilt SPO2&NIBP or facility of upgrading to these facilities
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PGI/MM/HEMA/15-16/04 ECG MACHINE 02 ECG Machine
Input circuit should be floating input circuit,protection from defibrillation
Lead should be Standard 12 leads
Acquistion mode should be 12 leads simultaneously
There should be standard A/D convertor- 12bits
The measurement Range should be 5mv PP
The time Constant should be 3.2 seconds
The frequency Response- 0.05Hz- 150Hz
The Callibration voltage should be in the 1mv +_ 3%
Sensitivity should be 2.5, 5, 10, 20(mmmv)
Input impedance >_50m amp
Input circuit current - <_50nA
Noise level - <12.5u Vp~p
Anti Baseline Drift -Automatic
Patient leakage Current <10uA (220-240V)
Patient Auxilliary current <0.1uA (DC)
Filter -EMG Filter 25Hz/45Hz/OFF DFT Filter 0.05/0.15/0.25/0.5Hz low PassFilter150Hz/100Hz/75Hz AC filter 50/60Hz
CMRR >110db
Recording mode Auto: 3CH,/2CH,3CH+1R,1CH,1CH+1R MANUAL:3ch,3/2CH,1CH.
Rhythm should be Single rhythm lead
Power Supply AC: 100V~115V/220~240V,50/60Hz Built in rechargeable Li-ion battery:Voltage 14.8V more than 3hrs.
Continuous operation under fully charged new battery Thermal Printer.
Record paper size should be more than 15 meters in length and approximately 80 mm wide.
Warranty as per institute norms.
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PGI/MM/HEMA/15-16/05 BEDSIDE ULTRASOUND MACHINE 01
PORTABLE ULTRASOUND MACHINE WITH COLOR DOPPLER
A state of art fully digital, compact portable colourdoppler ultrasound machine is required for bedside
diagnostic ultrasound with facilities for bedside ultrasound guided intervention procedures, with following
technical features.
Physical specification:
1. The unit should be compact, lightweight and portable. Specific weight and dimensions weight should not exceed 5Kg excluding cart and accessories.
2. Display:10.4" / 26.4 cm or larger diagonal high resolution flicker free LCD display with wide viewing angle 3. Laptop style Alphanumeric elastomeric QWERTY keyboard with splash resistant track pad /trackball with easy
access scan control 4. Transport trolley/ Mobility cart from the same manufacture should be provided with storage tray and at least
3 transducer holder 5. Multiple adaptor/ transducer connector for connecting at least 3 transducers with electronic switching facility
to toggle between transducers 6. Transport case or bag for transport without trolley should be provided to accommodate the system and
power cable, transducers and get bottle 7. System must have fast boot up to scanning in less than 30 seconds from off condition, for use in critical and
emergency situation in ICU. 8. Unit must be sturdy, resistant to breakage and damage on fall/ hit against the wall or hard surface 9. Demonstration of the system is must 10. it should be suitable for vasscular access (CVC placement) nerve blocks (lower as well as upper extremity) E-
FAST examination, abdonimal diagnostic ultrasonography and beside abdonimal intervention procedures, small parts both in adults and pediatric pateints and also suitable for echocardiography. Multiple preloaded application presets should be available.
11. USB port for connectivity to the computer. 12. System should have both European CE and US FDA quality approval and certification
Power requirement:
1. System must be able to operate on both AC and inbuilt battery pack. 2. Battery should have rechargeable Internal Lithium –Iron polymer battery. AC/DC poer adapter should be
provided for recharging the battery. 3. Battery be self recharging and should last at least for 45 minutes when fully charged under continuous use of
the system without AC 4. System with AC adapter and system with trolley/cart should function within 100-240 V, 50/60 Hz, AC, 5 amp
power outlets. Specify power requirements
5. System should be operational at 10-400 C and 15-95% relative humidity
System architecture, imaging modes and processing and archiving
1. Flat LCD/TFT Monitor of at least 10 inches 2. System should support broadband probes scanning with frequency range from 1-14 MHZ (±1 MHZ) 3. The system shall process a dynamic range of at least 165db 4. Imaging mode of real team 2 D, colour doppler, Pulsed wave doppler, continuous wave doppler, power
(energy) doppler should be available 5. Theunit must have real time compound imaging for improved contrast resolution and eliminating ultrasound
artifact to achieve optimum image quality on convex and linear transducers. 6. The unit should have automatic gain adjustment for B mode. 7. Scanning depth must be available up to 30 cm 8. Control for 2D mode. Total gain, depth, dynamic range auto gain 9. Controls for colour doppler: PRF, colour gain, position and size of ROI, steering of ROI, colour maps and colour
invert 10. Control for pulsed doppler: variable sample volume size from 1 to 5 mm or more, steer PRF, baseline, gain,
angle correction, spectral invert 11. Cine memory on all modes 12. On board storage of at least 1000 images. Storage in BMP and AVI format should be possible. Sorting of
database with pt. Name and date should be possible 13. The system should have Dual imaging, Duplex imaging, 2x pan/zoom capability 14. System should support the all DICOM functionality including storage, print and should be ready to connect to
PACS.
Transducers to be supplied:
1. Convex 2-5 MHZ. For general purpose abdonimal ultrasonography (older children and adults) 2. For pediatric abdomen: diagnostics ultrasonography and therapeutics abnormal interventions 8-5 MHZ; small
foot print size approximately 11 mm (optional) 3. High Frequency linear transducer 6-12 mhz. For vascular access, small parts, vascular, musculoskeletal
applications with Biopsy Guide facility 4. Phased array 2-4 mhz. Adult echocardiography, Fast applications
Optional Transducers/software/Items:
B/W thermal printer
Waranty:
The unit, transducers and all accessories should be covered with comprehensive onsite Warranty for five
years commencing from the date of issue of installation.
ESSENTIAL REQUIREMENTS:
The firm must have minimum number of 50 installations of the same model in India, attach list of
installations, and also provide performance certificates.
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PGI/MM/HEMA/15-16/06 ELISA READER 01
Specifications: Elisa Reader
1. Should be fully automatic and programmable to save multiple protocols.
2. Able to support all plate formats U bottom, V bottom and flat bottom 96-well micro plates.
3. Instrument should have spectral range from 400-750 nm.
4. Extensive on board assay configuration and read methods (End point, kinetic, spectrum, point to point etc).
5. Scanning time should not be more than 10 seconds.
6. Operating system should have temperature between 15-35 degree.
7. Instrument should have single and dual wavelength reading options.
8. User interface should be with LCD display with minimum programming steps.
9. Instrument should have external printer facility with USB port based printers.
10. Should have at least six standard absorbance filters.
11. Should have linearity and accuracy of ≤1.0%
12. Should have resolution of 0.001 OD and precision of 1.0% - 1.5%
13. Should be provided with computer system with a minimum of 18.5” display and software for data storage.
14. Warranty - Institute norms of 5 years
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PGI/MM/HEMA/15-16/07 TISSUE FLOATATION BATH 01
Specifications: Water bath/Tissue floatation bath
1. Tissue floatation bath required for flattening and drying tissue in Histo-pathological laboratories.
2. A rectangular water bath with Dimensions of approx 300-400 x 200-300 x 60-100 mm
3. Capacity of 2-4L.
4. Microprocessor based thermostat Control.
5. Digital display of temperature should be available. With temperature range from ambient to + 50°C -
+90°C.
6. Exact temperature constancy of ±0.5°C.
7. Power supply: AC line, 50 Hz, 220-240 Volts.
8. Warranty as per institute norms of 5 years.
PGI/MM/PATH/15-16/01 FROZER SECTION FACILITY (CRYOSTAT)
01
Equipment : Frozen Section Facility (Cryostat) against buy back of old cryostat
Specifications:-
1) Open top, heated sliding window, corrosion proof stainless steel cryochamber with good illumination
2) Microprocessor based touch key control panel with LCD display for all functions including of microtome.
3) Separate control for specimen head and knife edge temp. upto -300C or less.
4) Temperature control of cryochamber should be atleast -300 or less.
5) Preference will be given to models with dual compressor.
6) Facility for integrated quick specimen freezing upto -600C. Space for other specimen rack.
7) Removable section waste tray.
8) Automatic programmable defrosting with enclosed drainage system of defrost fluid.
9) Holders/carriers for holding and disposable high and low profile blades.
10) Specimen holder can hold specimen size up to 70x50 mm. Facility for both 3600 rotation as well as
movement in xy axis.
11) Automatic with motorized coarse feed and automatic specimen retraction on return stroke movement.
Facility for hand wheel brake
12) All standard accessories, tool kits and manuals to be provided with main equipment.
13) Also quote for 20 bottles of OCT media
14) CE / FDA certification compliance
15) Quote price in Indian rupee for the buyback of old non functional cryostat.
PGI/MM/MICRO/15-16/02 REAL TIME PCR MACHINE 01 Technical specifications for Real time PCR
Optical Unit:
Light Source: Tungsten halogen lamp; Five-excitation filters, five-emission filters and detection by CCD
camera
Thermal Unit:
Standard 96 well Plates & 0.2ml tubes Thermal Cycler.
Should be supported by 96 well plates,strips and tubes from the same manufacturer.
The operating temperature should be between 4 °C - 100 °C
Gradient temperature per column,
Chemistry: Open system, should support common chemistries like Taqman and SYBR Green.
The system should also be open for addition of new dyes without any filter change.
The system should be capable of multiplexing 5 targets per well.
The instrument must be calibrated for FAM/SYBR Green, VIC/JOE, NED/TAMRA/Cy3, ROX/Texas Red
and Cy5.
Software:
Licensed version of primer probe designing software and relative gene expression software should be
provided along with the system.
The software should enable advanced features like relative standard curve, import of unlimited number of
comparative Ct values to one study.
Normalization to multiple endogenous controls.
Simultaneous viewing of amplification plot, multi-component plot and QC summary within a study to easily
identify and eliminate outliers.
Sensitivity: The system should support detection of 1 copy of template in a 50µl reaction at least
99.7% or more confidence level.
Linear Dynamic range of 9 or more logs.
System Support:
A branded Laptop (e.g. HP/Dell) should be provided along with the system
Comprehensive warranty 5 years including calibration
UPS included
Training provision.
PGI/MM/MICRO/15-16/03 BIOMEDICAL WASTE COLLECTION BIN 40
TECHNICAL SPECIFICATION OF Bio Medical Waste Collection Bin:
1. Capacity: 60 Litre each
2. Set of Bins: 03 Nos.
3. Colour of Bins: Red, Yellow & Blue
4. Frame: Stainless Steel Frame
5. Paddle Lifting: Separate paddle lifting for each bin
6. Material of Bins: Plastic
7. Washable
PGI/MM/NM/15-16/01 INTERLOCK SYSTEM FOR WASTE GAS STORAGE TANK THROUGH RADIATION MONITORING DEVICES (CYCLOTRON FACILITY)
01
SPECIFICATIONS:-
Interlock system for waste gas storage tank (installed at cyclotron facility) through radiation monitoring
devices to control the radioactive gas release system as per AERB guidelines.
PGI/MM/NM/15-16/02 180 WATER PURIFIER SYSTEM (CYCLOTRON FACILITY)
01
SPECIFICATIONS:-
Recovered 18O water from the target implies several impurities such as organics and ions. Recovered water is
refined by the UV irradiation and the cold evaporation for reuse. Recovery efficiency of 18O water in shold
be more than 80 %. The system must consist of 2 units, i.e. Photox-unit, Evap-Cond unit. Normal capacity is
12gr/ day or higher.1) Photox Unit: Components: Quartz cells (10 pieces) with caps, a cell rack, a blower and
an ozone eliminator. 2) Evap-Cond Unit: System must be equipped with required glassware and Evaporation
glass ware & pot, a dewer flask, polystyrene tubes and a diaphragm vacuum pump.
PGI/MM/NM/15-16/03 WATER BATHS HEATING & RECIPROCAL SHAKING
01
SPECIFICATIONS:-
Rapid and accurate shaking by adopting silent and anti-vibration BLDC (Brushless DC) motors. And their
precise and constant temperature control provides ideal for sample. Bath Volume (L t.): 15.0 or more
Working Temperature Range (°C): Amb. +5 to 100 or higher; Temperature Stability (± °C): 0.2; Shaking
System Motion / Speed range (RPM) Reciprocating, 20 to 180; Recip stroke length (mm): 25, 30, 35;
Dimension Bath opening / depth (W x L,D)(mm ): 109 x 243, 235; Microprocessor PID control / automatic
tuning / calibration. Digital timer for delayed ON / OFF. (from 1 min to 99 hr 59 min) Protection against
over-temperature. Digital LED display. (0.1°C and 1 rpm resolution). Separate control keys for shaker
mechanism allowing the unit also to be used as a constant temperature bath. Isolated design of agitator,
heater, and sensor by a baffle plate to minimize the turbulence in the bath. fluid and also to protect users and
samples against direct contact. Removable shaking carriage designed for external assembly avoiding direct
contact with the bath fluid. Included SUS 304 spring wire rack with double-two-tier pro-viding various ways
of glassware settings. Clamp for various size of glassware must be given in the optional parts.
PGI/MM/NM/15-16/04 ULTRAVIOLET VIEWING CABINET 01 SPECIFICATIONS:-
Should be incorporate: 4 No’s x 15 Watt Tubes of 254 nm and with 1 no’s x 40 watt white light bulb.
Intensity at Bottom (µW/Cm²): 1750, Versatile, Simple change of the tube light when a new wavelength is
require. Removable box panel enabling positioning above a standard transilluninator. Viewing port with UV
absorbing filter.
PGI/MM/NM/15-16/05 LYPHOLYZER/FREEZE DRYER 01 SPECIFICATIONS:-
We require a compact, bench top, laboratory freeze dryer capable of removing water as well as organic
solvents such as acetone, acetonitrile, methanol, ethanol etc.
1. Upright stainless steel collector coil capable of removing 2.5 litres or more of water.
2. 24 hours and holding 4 litres or more of ice before defrosting.
3. Teflon-coated collector coil and chamber for processes involving corrosive compounds.
4. Dual 1/3 hp HCFC/CFC-free refrigeration systems to cool, collector to -80° C or below with drain valve
for disposal of defrosts material.
5. 12 or more ports Drying Chamber with individually controlled rubber valve & 20 port manifolds suitable
for drying in flask, tube, vials and ampoules.
• The body should be made of corrosion resistant materials.
• LCD display for system operating parameters, set-up parameters and alarm messages.
• System should have adequate safety features such as:
a. Alarm for abnormal system events such as: power failure, improper line voltage supply, collector
temperature rise above thresholds, service vacuum pump (after 1000 hours of vacuum use), and moisture in
collector.
b. Moisture sensor that prevents refrigeration or vacuum start-up when moisture is detected in the collector
chamber area.
c. Vacuum control valve that maintains set point vacuum level.
d. Vacuum break valve that bleeds air into the system when power to the freeze dryer or vacuum pump is shut
off.• Should have RS-232 interface option to connect with a computer.
Operating voltage, 230 volts, 50 Hz. All electrical parts should have CE Conformity and certification.
Vacuum Pump:
Suitable hybrid vacuum pump that is capable of delivering the maximum performance of the above specified
Freeze dryer. The vacuum pump should have the following features:
1. Designed for use with acids and other harsh chemicals present in samples.
2. Hybrid pump system consists of a two-stage rotary vane pump and two-stage, chemically-resistant
diaphragm pump or better.
3. The pump should have the vacuum capabilities of a rotary vane pump combined with the solvent and acid
handling capabilities of a PTFE diaphragm pump.
4. Low maintenance, longer lasting.
5. Ultimate vacuum (partial pressure) 2 x 10-3mBar or better
6. Suction of 95 litre per minutes or better.
7. Electromagnetic pressure control for vacuum control.
8. Should have vacuum break valve to prevent oil back streaming.
9. Vacuum pump should be supplied with one litre bottle of high quality vacuum pump oil, power switch,
powercord and plug. Operating voltage, 230 volts, 50 Hz.
11 All electrical parts should have CE Conformity and certification.
Essential accessories:
40ml flask, 12 nos.; Tube holder to accommodate up to 30 no. of 2 ml tubes.
SS flask top to valve 12 nos; Activated Carbon Solvent Trap - to prevent migration of organic solvents into
pump interior. Replacement Media for charcoal solvent trap; Unit should be accompanied with Data logger &
software
Optional accessories:
1. Flask of following capacity along with adapter to connect the flask with drying drum – 80 ml, 150 ml, 300
ml, 750 ml, 900 ml, & 600 ml
PGI/MM/NM/15-16/06 HOT AIR HEATING AND DRYING OVEN (CYCLOTRON FACILITY)
01
SPECIFICATIONS:-
Volume : 150 Lt. or higher, Should be operated on 230V, 50Hz single phase AC supply and having temperature
ranging between 50-300ºC; ; Forced Convection Pre Heat Technology. Should be made of double walled
chamber -Inner made of stainless steel SS 304 grade. Electro-galvanised steel with white oven-baked epoxy
antimicrobial powder-coated finish. Single piece 304 Grade stainless steel chamber with rounded corners.
Heat resistant enamel painted steel exterior with coated aluminum trim. Low watt density, long life heating
element. Should be provided with air circulating fan on top Forced convection system ensures good mixing,
strong dispersion and maintains higher temperature uniformity inside the chamber. Should provide with a
variable microprocessor based digital temperature controller with digital display and on screen prompt,
thermometer should be provided separate. Should have a minimum chamber size of (L*B*H) 18*18*26 with
3 stainless steel adjustable shelf heights. Fiberglass gasket with stainless steel mesh core to prevent heat loss,
Should provide with air ventilations.
PGI/MM/NM/15-16/07 CENTRIFUGE 01 SPECIFICATIONS:-
Maximum RCF : about 20,913 x g
Maximum RPM : 100-14,000 rpm
Fixed Angle Aerosol Tight Rotor for 18 x 1,5ml/2 ml
Acceleration time to max. speed 11 s or higher
Braking time from max. speed 12 s or higher
Short-spin function with Soft ramp , Automatic lid opening
Low access height of 26 cm, refrigeration unit should be at the rear of the unit. Noise level <56 dB(A) or
less, A pack of 1.5mL Eppendorf tubes to be quoted with instrument.
PGI/MM/NM/15-16/08 ORGAN LEVEL INTERNAL DOSE ASSESSMENT (OLINDA) FOR THE INTERNAL DOSIMETRY
01
SPECIFICATIONS:-
OLINDA/EXM personal computer code (three users) for calculating organ doses and effective doses in
nuclear medicine studies is available for distribution. OLINDA/EXM, which stands for Organ Level INternal
Dose Assessment/EXponential Modeling, calculates radiation doses to different organs of the body from
systemically administered radiopharmaceuticals and performs regression analysis on user-supplied biokinetic
data, to support such calculations. Compatible for Window-2000, Window-2007, 2008 or higher version of
operating procedure. Branded computer system with i3 processor, window 7 or higher version operating
system, 6 GB or higher RAM and 1Tb internal hard drive, 19 inch or higher LED display monitor.
PGI/MM/NM/15-16/09 MICROWAVE SYNTHESIZER 01 SPECIFICATIONS:-
A Microwave synthesizer with best in class safety for operations (certificate to be provided) at elevated
temperatures having capacity of microwave power output of 300 watts or more with the monomode
microwave applicator Built in operating system with fluorescent in built display with alpha-numeric keypad
for entering the parameters System must operate stand alone as well as through PC suitable software with
standard USB port Interfaces System Software must automatically adjust the power delivery based upon
sample Load and pre-programmed control settings.
Pressure range: 0-35 bar
Temperature range: more than 300 oC (should have option of carrying reactions at sub-ambient temperatures)
Infrared temperature control or fiber optic control
Standard cooling facility along with cavity cleaning facility in case of spillage
Built in stirring option: In situ magnetic variable speed Vessels:
(a) Pressurize vessels of following should be offered Volume: 10mL and more than 40 mL capacity, Pressure:
30 bar or more
MOC: Glass No. of Vessels: 500 Nos. Vessel should be of vent & reseal technology and reusable
(b) Normal pressure reaction vessels: 100 mL glass vessel at least 15 nos
System should be provided with pressure sensor.
Working volume: 10 ml (or more) to 80 ml (or less). Different size of 50 numbers of magnetic stirring bars
should be provided to perform reactions under stirring condition. The system should have facility to use
different sizes of reaction vessels in microwave and the minimum reaction volume is at least 0.5 ml. 100
numbers of snap caps should be provided if required. At least 100 numbers of 10 ml (or higher) vessel, 10 no
of 30 ml vessel with caps (with provision of attaching 30 ml vessel), and 5 numbers of 100 ml (or more)
vessel (for large scale reaction) should be provided with the instrument.
Optional: An auto sampler with more than 10 positions to carry the reactions at a time.
The system should be provided with all other necessary accessories that are required for catering the needs in
regular operations as optional.
PGI/MM/NM/15-16/10 PREPARATIVE FLASH CHROMATOGRAPHY SYSTEM (CYCLOTRON FACILITY)
01
SPECIFICATIONS:-
High performance preparative chromatography flash system which allows running both flash and preparative
high performance preparative chromatography separations;
Pumping System
• Must have two Piston pump; Flow rate up to 220 mL/min or higher,
• Pressure range up to 80 bar or higher; Should be Quaternary gradient and have selectable Air Purge (for
flash cartridges).; Should have inbuilt solvent leak sensor.
• Adjustable mixing volume for optimum gradient performance.
• Should have compatibility with Flash cartridges, Glass columns and HPLC columns having a diameter up to
70 mm or higher with silica particle size down to 9 or lesser micron meter.
Injection valve Should be delivered with 6-port electrical injection valve as a standard function. Liquid or solid sample
injection. Should have Automatic Injection valve: 6 way 2 - position injection valve with injection loop.
Detector: UV/Vis diode array detector equipped with a deuterium discharge lamp.4 wavelengths with
SCAN function. Range 200 - 600 nm. Accuracy of adjustment ± 1 nm; Reproducibility ± 0.5 nm ;Flow cell
path length 0.3 mm Noise level at test cell ± 5 x 10-5 AU at 254 nm, TC 0.75 s; Drift at test cell (254 nm
after 1 h) 1 x 10-3 AU/h; Time constant (T90) 1 s; Light source Deuterium discharge lamp; Maximum flow
rate 400 mL/min or higher; Maximum pressure at the cell 15 bar / 290 psi or higher; Output for integrator at
least 1 V/AU (in digital form only). Fraction Collector: Rack for 18 x 150 mm or 18 x 180 mm tubes, 64
positions, 100 Glass tubes, 18 x 150 mm; Possibility to create regular racks (Customized). Should be
supplied with 2 racks with Integrated waste valve. Any up gradation in software should be provided free of
cost.
Display and Software
• Integrated touch Screen Interface; Operating system: Windows 7 or higher version; Corresponding
Software
• Preparative columns: silica based columns (one each): dimension 4.6mm X 250 mm (5m); 10.0 mm X
250 mm (5m) and 30mm X 150 mm (10 m) AND C-18 Based columns (two each) dimension 4.6 mm X
250 mm (5m); 10.0 mm X 250 mm (5m)
Glass Columns: Should be supplied with one set of glass columns for sample range 1gm, 10gm, 20 gm and
50 gm. Length- 100 mm - 460 mm.
Silica High performance cartridges: for sample size of 4 g (100 No.), 25 g (100 No) /80 g (50 No) and
120 gm (20 no.)
All necessary accessories and spare which does not cover in standard warranty should be quoted separately
as optional items and prices separately.
PGI/MM/NM/15-16/11 INFUSION PUMP WITH LEAD SHIELDING
01
SPECIFICATIONS:-
Microprocessor controlled syringe pump must be US-FDA /CE / IEC approved. Rated voltage 220–240;
Battery backup for at least >3 h; Wide LCD display with provision to display: Adequate lead shielding for
delivery of Lu-177, Tc-99, 131-I and radio isotopes labelled drug for therapy Drug name; Flow rate; Total
infused volume; Battery indicator; Should have KVO; Should have anti bolus system; Should have
programmable occlusion pressure: Low; Medium or high; Should have following audio –visual alarms;
volume limit pre alarm; Occlusion; PM line disconnection; Low battery; Mains disconnection; Incorrect
syringe placement ; Drive disengaged ; internal function; Delivery range0.1 –999.9 ml /h; Bolus range 1.0 –
1200.00 ml /h; Should have universal mounting accessory on both vertical and horizontal; On line changing
of delivery rate possible; Syringes size 2.0 ml, 3.0 ml, 5.0 ml, 10.0 ml, 20.0 ml, 50.0 ml; Drive accuracy
should be +/-1 %; Machine should be able to get configured in standby mode. List of consumables, if any
with price frozen for 5 years should be quoted separately. Bidder should submit user satisfactory reports for at
least two institutes / hospital of repute. PGI/MM/CSSD/15-16/01 WHEELED BINS FOR HOSPITAL
SANITATION (MATERIAL:HDPE)
PGI/MM/PH. T./15-16/01 ELECTROTHERAPY/ COMBINATION THERAPY 02
*Modern, Computer based,12” Touch Screen display, Multi-Channel, max variety of current output e.g. IG, G, SF, F etc. *Diagnostic / Therapeutic. *Pulse duration of 0.01,.03,0.1,0.3 ms. Parallel, separate and alternate applications, all low and medium frequency currents with option of adding Galvanic component to other current forms for better pain control. With ULTRASOUND facility having multiple choices of penetration depth and choices of
mechanical and thermal effects separately. Continuous & Pulsed ultrasound therapy with multi-frequency treatment head for 1
and 3MHz with contact control facility, automatic power switch off and treatment time interruption in case of insufficient contact. * Connection facility for second treatment head.
*Provisions for quick and simple combination of ultrasound with several current types. PGI/MM/PH. T./15-16/02 SHORT WAVE DIATHERMY 02
Microprocessor based continuous/pulsed short wave diathermy unit for superficial and deep tissue treatment with following features- *working frequency : 27.12 MHz *pulsed output:100W *Continuous output: 470W
THE MATERIAL OF THE BINS ARE HDPE.
THE FIRMS CAN OFFER THE RATES AND CAPACITY OF WHEELED BINS OF SMALLER CAPACITY ALSO.
*Protection class: CEI 62-5: 1 BF *Tuning : Automatic *Frequency: 20-200 Hz,*Impulse length : 400 ms,*Display: LCD,*Dimension: cm 40x37 x95h
PGI/MM/PH. T./15-16/03 DECOMPRESSION THERAPY SYSTEM 01
Traction system with multi joint adjustable bed having provision of cervical as well as lumber skeletal traction, with Bolster less leg elevation system for supine treatment and whole body vibration, lower section locking and unlocking system with multiple traction
speed like slow, normal, fast with user definable hold, rest, treatment time. PGI/MM/PH. T/15-16/04 GUTHERIE SMITH’S SUSPENSION FRAME 01
Modern designed with all accessories
PGI/MM/PH. T./15-16/05 SHOULDER WHEEL EXERCISER 02
Height and radius adjustable
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