mmo 6000 - joerns.nl · 8.2 articulation of the bed deck 8.2.1 electric backrest this command...

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USER MANUAL TECHNICAL MANUAL

PARTS LIST

MMO 6000

Version 3

18/11/2016 DOC 1521013

Modifications – Version 3.2 - 29/06/2018 Brake pads cleaning : page 14

Brake module : spring of the mechanism : page 31

Warranty conditions page 36

Translation correction All pages

Spare part list Update : pages 41 to 52

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Sommaire 1 Symbols used in the manual ..................................................................................... 4 2 Intended use of the bed ........................................................................................... 5 3 General information ................................................................................................. 5 4 General precautions for use ...................................................................................... 6

4.1 Potential Risk of Entrapment .............................................................................. 7 4.2 Transport and storage ....................................................................................... 8 4.3 Installation and commissioning ........................................................................... 8 4.4 Identification of labels ....................................................................................... 8 4.5 Warranty terms / after sales service .................................................................. 10 4.6 Certified features ............................................................................................ 10

5 General Cleaning of Bed ......................................................................................... 11 5.1 Recommendations ........................................................................................... 11 5.2 Procedure ....................................................................................................... 11

6 Bed features .......................................................................................................... 14 6.1 Symbols & pictograms of remote control ........................................................... 15 Accessories ................................................................................................................ 17 Removal of head/foot board ......................................................................................... 18 6.2 Split siderails .................................................................................................. 18

7 Product description ................................................................................................ 19 7.1 Dimensions ..................................................................................................... 20 7.2 Technical specifications .................................................................................... 20 7.3 List of parts covered by ISO 60601 ................................................................... 21 7.4 Maintenance specification for electronic parts and actuator (LINAK) .................... 22

8 Use of different product features ...................................................................... 23 8.1 Variable height ................................................................................................ 23 8.2 Articulation of the bed deck.............................................................................. 24

8.2.1 Electric backrest ....................................................................................... 24 8.2.2 Operating the safety flattening of the bed when the power supply is cut ....... 25 8.2.3 Operating CPR function with a patient in bed: ............................................. 25 8.2.4 Electrical thigh section and manual calf section ........................................... 26 8.2.5 Comfort position ....................................................................................... 26 8.2.6 Storing the bed exit height into the electronic memory ................................ 27 8.2.7 Front bed exit and Chair position - 1 button operation ............................... 27 8.2.8 Trendelenburg/Reverse Trendelenburg Position .......................................... 28 8.2.9 Electric CPR Function ................................................................................ 28 8.2.10 Under bed night light ................................................................................ 29 8.2.11 Wall protection and position indicator (option) ............................................ 30

8.3 Brakes ............................................................................................................ 31 8.4 Transferring the patient in the bed ................................................................... 32 8.5 Moving the bed ............................................................................................... 32 8.6 Patient restraint .............................................................................................. 32 8.7 Reset procedure .............................................................................................. 33 8.8 Calibration procedure – loss of Variable height position ...................................... 33 8.9 Calibration procedure when overloaded ............................................................. 33 8.10 Handling siderail: ............................................................................................ 33

9 Accessories ........................................................................................................... 34 9.1 Gap filler ........................................................................................................ 34 9.2 Head /Foot board support ................................................................................ 34 9.3 Flexible holder for hand pendant ...................................................................... 35 9.4 Siderail padding .............................................................................................. 35

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9.5 Patient Lifting Pole .......................................................................................... 35 9.6 IV pole ........................................................................................................... 35 9.7 Remote and Hand control holder ...................................................................... 36

10 Warranty and Installation .................................................................................... 36 10.1 Warranty ........................................................................................................ 36 10.2 Installation and commissioning ......................................................................... 37

11 After sales service .............................................................................................. 38 11.1 Troubleshooting .............................................................................................. 38 11.2 Conditions of on-site assistance and spare parts supplies .................................... 38 11.3 BED IDENTIFICATION LABEL ........................................................................... 39

12 Exploded view of the bed .................................................................................... 40 13 List of the spare parts ......................................................................................... 41 14 Maintenance guide for medical beds Levels 1 & 2 .................................................. 52

14.1 Manufacturer’s commitment: ............................................................................ 52 14.2 Organization of services: .................................................................................. 52 14.3 Preventive maintenance ................................................................................... 54

15 Servicing ............................................................................................................ 57 15.1 First Level diagnosis ........................................................................................ 57 15.2 Second Level – wiring diagram ......................................................................... 59

15.2.1 Replacement of the patient hand pendant(refer to wiring diagram) ............... 61 15.2.2 Replacing the control box .......................................................................... 61 15.2.3 Replacing the electric actuators ................................................................. 61 15.2.4 Replacing the castors ................................................................................ 62 15.2.5 Replacing the CPR cable ............................................................................ 62 15.2.6 Replacing a backup battery ....................................................................... 62

16 Data .................................................................................................................. 63 16.1 Electromagnetic compatibility ........................................................................... 63 16.2 Disposal at end of product life .......................................................................... 66 16.3 Earthing ......................................................................................................... 66 16.4 Life of the device ............................................................................................ 66

17 Manufacturer’s detail .......................................................................................... 68

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1 Symbols used in the manual

Warning, please read this instruction regarding safety.

Index of waterproof resistance of the electrical components

Protection against electric shock.

Type B device according to EN 60 601-1

DC power

AC power

250 kg: Symbol safe working load of 250kg

220 kg: Symbol maximum patient weight of 220 kg (ca. 30 kg for mattresses and accessories)

Device of Class II double insulated

Risk of crushing feet

Risk of crushing hands

Read user manual

Max working load in Kg

Dimension of mattress compatible with the bed

Compliance: following European Directive No. 93/42/EEC (medical devices)

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2 Intended use of the bed

This bed is designed for use in hospital and nursing homes. It is designed to enable comfortable sleeping and smooth traveling in or out of bed. This bed ensures the best provision of care for both patients and staff. This type of bed is made for use in an environment of class 2 (short term care services or other medical infrastructure). This bed is designed for short term care in medical institutions. Where medical care, medical supervision and control is provided if necessary and where Electro Medical devices used in medical procedures can be provided to help maintain or improve the patient's condition. Such institutions are hospitals, nursing homes for long durations, rehabilitation centers, geriatric centers and other specialized care centers. This bed is intended to be moved only in the patient room for cleaning or for care giving.

3 General information

We hope that this product will give you complete satisfaction. In order to use the bed in the best conditions of safety, we advise you to read this manual before commissioning. Parts of the bed that may come into direct or indirect contact with the tissues, cells or biological fluid of the body are head and footboard as well as protective barriers. This bed meets the requirements of NF EN 150 10993. The mattress used must also meet the requirements of this standard. The MMO 6000 is available with an integrated AeroSpacer mattress in the UK and EIRE.

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4 General precautions for use

The use and handling of a medical bed can cause injury. It is essential that the person who is handling the bed is authorized and trained. This person must know the consequences of all actions and how not to cause involuntary movements.

Any maintenance must be performed by qualified personnel.

Upon moving the bed in a room, keep sufficient space to allow for the movement of the bed and avoid damaging the environment or injuring a person. To avoid risk of fire, when the actuators of the bed are used too intensively, the bed can go into "safe mode" and shutdown. The bed will return to its normal functions after returning to normal temperature. This return to normal may take several hours. Time of usage taken into account for the thermal safety is 10% or 6 minutes use per hour.

DANGER: The MMO bed is an electrical device with a risk of electric shock. Personnel using the bed must be informed and trained to potential risks related to electrical appliances. It is essential to know how the product works to achieve the desired result during handling. It is essential to comply with the use and recommendations described in this

manual to ensure the security and integrity of the different users.

The bed is not explosion-proof equipment and cannot be used in explosive areas. Actuatorized bed mechanisms can cause serious injury. Do not put arms or legs in the side rails. During operation of the actuator make sure that nobody is under the bed, and no pet or object is in the mechanism. Adopt special measures for safety in case of use of bed by confused patients (lower position, safety mats, protective covers barriers, enhanced surveillance). The side rail should be fully up and locked or fully folded to avoid risk of entrapment. Avoid floor coverings that are too soft or improperly installed, which can be degraded by the bed.

WARNING: during the use of the bed with other medical equipment, it is necessary to check compatibility. It is also important to check that the equipment is compatible with the official medical norms. It is necessary to keep the plug accessible at all times to be able to unplug the bed quickly, in case of emergency. It is necessary to use only MMO accessories

IT IS STRONGLY RECOMMENDED NOT TO: Smoke in or near the bed Use the bed for a child under 12 years of age or smaller than 146 cm Sit on the bed if that section of the bed is not completely flat Load the bed beyond the safe working load of 250kg, also not to operate under

these conditions Use electric functions permanently or too intensively and without respecting

the duty factor of 10% or 6 minutes usage per hour.

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IT IS STRONGLY RECOMMENDED NOT TO:

Use accessories that do not come from the manufacturer of without a specific agreement

Pass the power cord into the moving parts of the bed or castor areas (to avoid entrapment or damage)

Use the bed if the power cord is damaged Clean the bed with water under pressure To carry out cleaning or maintenance without the bed being unplugged from

power supply

Use any electrical functions on the bed if potential presence of flammable gases such as anesthetic agents etc.

To use the electrical functions of the bed in an surgery operating room To use the bed if it has a mechanical or electrical malfunction

Ensure that the use of the bed is compatible with the medical condition of the patient. See conditions for use of various functions of the bed in the corresponding chapters. Regular use of the bed with a load greater than the safe working load of 250kg can degrade components prematurely and cause serious failures. Please ensure any power cables are not trailing beneath the bed, especially during transportation of the bed, this could result in damage to the cable.

4.1 Potential Risk of Entrapment

The bed has been designed in accordance to ISO 60601 standards to reduce or eliminate risk

of entrapment and/or injury.

The space between the calf section on the leg section is less than 25mm

The space between the brake pedal and the floor is approx. 25mm (with 100 mm castor fitted)

The space between the split side rails and the floor is approx. 120mm

The space between corner of the bed and the floor is approx. 120mm.

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4.2 Transport and storage

The bed is designed to operate at a temperature between 5°C and 40°C. These conditions should be applied during storage and transport. For transport the deck must be flat in the low position and all functions must be locked and the wheels braked. The bed should be protected from impact and friction. It should be strapped. Do not use a fork lift. The bed must have paddings. Beds should not be stacked on top of each other. There should be no load of any type on the bed during storage. It is recommended after a storage period and before the first use, to leave the bed at room temperature for some time (approx. 5 hours) before verifying its operational state.

4.3 Installation and commissioning

A new bed arrives with the backrest and accessories dismantled, bed sections securely strapped, packaged in protective wrapping. If the installation is not done by us, please proceed as follows: 1/ Remove the protective elements and clamping (red cable ties). 2/ Set backrest and accessories (as shown in the corresponding chapters). 3/ Connect the power cord located on the headboard to the 230V/50Hz or 60 Hz network. 4/ Check all pin connections are present, that the cables are not pinched and that the power cable is not strained. 5/ Connect the power cord (located at the head end of the bed) to the mains power socket. 6/ Perform a thorough cleaning of bed before the first use (see Section 5, Cleaning). 7/ Upon placing the bed in a room, ensure there is sufficient space to accommodate different movements of the bed and to avoid damaging the environment and/or injury to patient or caregiver

Grid Connection: Make sure the power supply complies with the safety standards enforced, especially as the supply voltage is 100-240V/50-60Hz + / - 10V and that there is a ground plug. Check that the power plug is properly connected. It is strongly recommended to connect the bed via a protective 30mA RCD ≤ to identify any electrical failure of the product. An equipotential terminal to ground the bed is situated under the deck.

4.4 Identification of labels

Reference label of the manufacturer’s type and number of the bed

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Label: risk of crushing the foot

Label: risk of crushing fingers

For 3 bars side rail, mattress max thickness is 17 cm For 4 bars side rail, mattress max thickness 26 cm Width of mattress : 90 cm Length of mattress: 200 cm

Unused connections are sealed to prevent damage from electrostatic discharge. Do not change the configuration of the bed without the permission of the manufacturer. Do not pull the mains cable to remove the plug from power outlet. Users (patients and their families) should be informed of safety rules to comply with when using the bed.

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The bed comes with a simplified user guide

4.5 Warranty terms / after sales service

Our metal frames are guaranteed for a period of 10 years. Excluded from this warranty: all electromechanical parts (motors, gas and electric actuators, remote control, hand pendant, wheels, hospital beds, thermoformed plate). All of these parts are guaranteed for 3 years. A technical team is at your service 24h/27, 365 days a year to advise you and decide the appropriate response to a problem. Warranty Terms and Conditions for UK and EIRE MMO and Medstrom offer a 10-year warranty on metal frames, backed-up with a 5-year warranty on all electrical parts. This is a no-quibble warranty on the condition that a Medstrom-approved maintenance programme is in place utilising approved OEM parts and that the product is not subject to use beyond the manufacturer’s guidelines and normal wear and tear. For UK and EIRE customer, if no service contract is in place within the first year of purchase, the warranty will revert to two years only. INVALID WARRANTY IN THE FOLLOWING cases:

Disassembly of mechanical or electrical parts of the bed without consultation and approval from the manufacturer

Use of replacement parts that are not supplied by the manufacturer. Rework on any electrical parts or gas cylinders. Degradation of coatings or materials from shock, friction and scratches. Abnormal use of bed, not following the precautions and recommendations which result

in degradation of the bed or its environment.

Using cleaning or disinfecting products discouraged by the manufacturer (see chapter 5, Cleaning)

Using washing machine or washing with excessive amount of water or using a pressure jet.

Crushing or cutting the power or the control box cords. Intensive use of electric bed functions beyond the recommended service interval

Unused connections are sealed to prevent damage from electrostatic discharge. Do not change the configuration of the bed without the permission of the manufacturer. Do not pull the mains cable to remove the plug from the main power outlet. Users (patients and their families) should be informed of safety rules to comply with when using the bed. The bed comes with a simplified user guide The manufacturer, assembler or installer does not consider itself responsible for the effects on safety, reliability and features of the device if the electrical wiring of the building does not comply with the relevant requirements and if the bed is not used in accordance with the instructions for use.

4.6 Certified features

Certified characteristics are safety, electromagnetic compatibility, mechanical safety and fitness for use of the bed and its accessories.

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5 General Cleaning of Bed

The bed is not designed for automatic cleaning but only for manual cleaning only

5.1 Recommendations

Whenever cleaning the bed, it is advisable to follow the following recommendations:

Unplug the bed and lock all functions if the bed is equipped with a battery (if the bed is unplugged, check that the plug does not come into contact with liquids).

Check that electrical connections are secure. Check that electrical components do not show any signs of wear likely to allow the

penetration of liquid. Do not wash the bed in a wash tunnel, using a water jet or with any sort of pressure

equipment.

Avoid saturating areas containing electrical connections or electrical components. Be sure to carefully dry areas cleaned to avoid any risk of moisture remaining, in

particular in the area of electrical connections.

If there is any doubt about the penetration of liquid into the electrics, it is strongly recommended that the bed should not be reconnected to the mains electrical supply and the maintenance department should be advised.

• Clean surfaces with a soft cloth, warm water and a mild detergent/disinfectant. Ideally use the cleaning/disinfection solution recommended by the hospital, following the dilution instructions carefully.

• Products on the “positive list of disinfectants” drawn up by the SFHH (French Society of Hospital Hygiene) are recommended by the manufacturer.

• The use of abrasive products or materials is forbidden.

• Products such as petrol, ketonic solvents, concentrated alkali or acid products, chlorine based solvents or dissolvent risk causing permanent damage to the surface.

• Non-ionic detergents diluted to 5%, bleach diluted to 10%, ammonia based products diluted to 5% may be used.

• Stains left by coloured substances such as eosin, betadine, etc. as well as food products should be cleaned as quickly as possible so as to avoid the risk of impregnation.

• For stubborn stains, the use of pure disinfection products is possible locally as long as the necessary precautions are taken.

• Areas showing traces of cuts or deep scratches should be repaired so as to avoid the risk of infiltration and deterioration of the protective surface.

5.2 Procedure

• Healthcare establishments are divided into sectors in terms of the risk of infection. • Frequency and methods of cleaning and disinfection are adapted according to the

evaluated risk.

• The level of infection risk in one room with a patient being cared for is moderate. It is much higher if the patient presents an identifiable infection risk.

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• Cleaning or disinfection of a medical bed, although not in direct contact with the patient and in particular damaged areas, should be cleaned regularly. Certain areas of the bed are more subject to contamination given the frequency of contact with carer’s and patient’s hands. The bed can be broken down into 3 types of area:

•

High contamination level o Bars of the head/foot boards. o Side protection devices o Manual and electrical control handles. o Accessories (arm, intravenous stand, urine sac support, etc.)

Moderate contamination level o Bed head/foot boards o Upper surface of the bed o Brake control pedals o Corner protectors

Low contamination level o Metal structure of the bed o Inside surface of the bed o Electric actuators o Wheels

Sources of dirt and contamination of a medical bed in use are: fabric dust coming from the bedding, food residues, ink, antiseptic liquid, vomit, urine, excrement, blood, etc. It is therefore necessary to take 3 types of cleaning/disinfection or bio-cleaning of the bed into consideration. Daily bio-cleaning of the areas of high risk. Bio-cleaning at the start and on the transfer of the patient and as a minimum, every month for high and moderate risk areas. Full bio-cleaning of the bed after the departure of a patient presenting risk of infection and as a minimum, every two months. DAILY BIO-CLEANING PROCEDURE This procedure can be carried out with the patient still in the bed, the objective being to ensure good hygiene of the parts regularly in contact with caregivers and/or patients hands. Carefully clean the bars of the head and foot boards, the side protection devices, the handles of the manual controls, the handles of the electric controls and their cable, the arm, the intravenous stand and the urine bag support. Eliminate all traces of dirt apparent on the other parts of the bed.

Using detergent/disinfectant products does involve some risk. Always wear Personal Protective Equipment (PPE), follow the instructions and avoid mixing products.

BIO-CLEANING PROCEDURE MONTHLY OR ON THE DEPARTURE OF A PATIENT This procedure is carried out without a patient in the bed. The objective being to disinfect all parts of the bed that regularly come into contact with hands, as well as areas dirtied by liquid deposits, secretions, dust and food residue etc.

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• Use a swab and the detergent/disinfectant solution approved by the establishment. • Put the bed in the flat position and the bed base at the pelvis position (using the neutral

position control if the bed has one), unplug the bed and lock all electrical functions, unlock the brake, move the bed away from the wall to give access all around the bed, and reapply the brake.

Cleaning the bottom part of the bed:

• The foot board, cross-member taking the foot board, all stops, caregivers control and the tidy tray.

• Lift one half of the mattress and fold over the other part, clean the upper surface of the bed as well as the sides, then underside of the mattress and fold it. Carry out the same procedure for the other half.

• Clean the top of the mattress, electric control unit handle and cable, orange handles and urine bag supports on either side.

Cleaning the top part of the bed:

• The bed head, the cross-member taking the head board, the stops, the arm, the intravenous stand.

• Unlock the brakes, reposition the bed against the wall, lock the brakes again and clean the brake control bar.

• Reconnect the bed and unlock the electrical functions. FULL BIO-CLEANING PROCEDURE FOR THE BED This operation is carried out without the patient in the bed. The objective is to disinfect the whole bed after it has been occupied by a contaminated patient or periodically every two months. This operation should also be carried out before first using the bed

• Use a swab and the detergent/disinfectant solution approved by the establishment. • Remove the mattress, the various plastic parts of the bed (warning: the central part

protects the power supply unit, its connections and two sensors) and the head/foot rests.

• Adjust the bed base to pelvis height and raise all the hinged sections using the control handle. Unplug the bed and lock all the electrical functions, unlock the brake, move the bed away from the wall to give access all around the bed and reapply the brake.

Cleaning the bottom part of the bed:

• The cross-member taking the foot board, all stops, the carer control and the tidy tray, the bed extension.

• Clean the curved tubes that make up the bed, the bed base, the grey power supply unit (be careful not to disturb the sensor settings or disconnect any cables), the grey sheathing, the electric actuators, the orange handles, the urine bag support and the control unit as well as its cable.

• Clean the upper part of the bed: Cleaning the upper part of the bed:

• The head rest, the cross-member that takes the head rest, the stops, the arm and the intravenous stand.

• Clean the bed chassis, the elevation arms, the wheels, the base cover and the wall stop.

• Clean both surfaces of the various plastic parts of the bed base and put them back in place (be careful to make sure they are positioned correctly on the curved tubing).

• Clean the head/foot boards and reposition them on the bed.

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• Unlock the brakes, reposition the bed against the wall, lock the brakes and clean the brake control bar

• Reconnect the bed to the main control power supply, unlock the electrical functions and return the bed to the flat position using the control handle.

• Clean the mattress and replace it on the bed. To ensure safety while using the bed, the brake pads should be cleaned with a small clean and dry cloth every two months. The bed should not be braked to carry out this operation. (See photo)

Re-connect the bed and unlock the electrical functions.

6 Bed features

The bed has a number of features as standard: • Electric or manual backrest with CPR function • Electric or manual thigh section with fixed manual calf section • Split side rails - Hand control, and / or satellite control box and/or caregiver control box at the foot of

the bed with or without infrared remote control (Infrared remote control not available in the UK or IERE).

• Castors 100 mm with or without fairing for cleanliness • Bed weight without accessories, with type A boards and side rail : 175kg • Basic version has straight castors 100mm on head and/ or mono block manual leg

section

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NUMBER NAME

1 Backrest

2 Thigh section

3 Calf section

4 Footboard

5 Headboard

6 Brake pedal

7 CPR handle

8 Split siderail handles

6.1 Symbols & pictograms of remote control

Infrared remote control .Hand pendant 5 functions with lockout function

Satellite hand pendant

Backrest

Thigh rest

Comfort position

Trendelenburg Reverse

trendelenburg

CPR electric

Backrest

Height

Thigh rest

Comfort position

Trendelenburg Reverse

trendelenburg

Backrest

Backrest + Thigh rest = comfort chair position

Thigh rest

Height

Light under the bed

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Control panel at the foot of the bed for caregiver with central lockout

NOTE: The wireless remote control is universal. It allows controlling of all MMO 2000, 3000, 5000, 6000 or 8000 beds to the extent that they are equipped with the infrared receiver. The use of two types of remote control is also possible on the same bed.

Caution: Do not use wireless remote control in rooms equipped with several beds. In case 2 beds with remote controls are present in the same room, 2 beds will be operated simultaneously at the same time. This presents a risk for the patient. For proper operation of the remote no obstacle must interfere with the infrared receiver located at the head of the bed. Point the remote control in the headboard

direction.

Selective lockout of the electric functions The hand pendant has a selective lockout function allowing to block independently any electric function of the bed.

Warning: for irregularly monitored patients, it is advisable to leave the bed in a low position to reduce the risk of injury in case of falls. Under certain circumstances it may be necessary to prevent operation of the bed

controls, therefore we recommend you use the lockout functions.

To selectively disable bed functions on the handset: use key supplied, engage key in desired lock location point. Turn clockwise to lock desired function. Turn anti-clockwise to unlock

CPR Electric

Lockout

Battery led

Backrest

Height Thigh rest

Comfort

position Trendelenburg/

Reverse Trendelenburg

Under bed light

Lockout

Set Patient exit height

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Condemnation is a mechanical device that acts only on the hand pendant. The remote control, always allows the use of the locked function. For electric locking,

use the caregiver’s control box at the foot of the bed.

The caregiver control box allows a selective locking of function. This allows the patient to control certain function of the bed but not all according to his injuries. If the bed is equipped with a satellite control pendant, an orange dot lights up on the locked function.

Warning: for irregularly monitored patients, it is advisable to leave the bed in a low position to reduce the risk of injury in case of falls It is essential to use the lockout function devices to lock out the functions and the

wireless remote should not be removed.

Accessories

MMO bed is equipped with devices to receive accessories:

2 x sockets for patient helper between the headboard and backrest. 4 x sockets for IV pole located at the head and foot section of the bed (2 at head

section and 2 at foot section)

KEY

Exemple :

Back rest + lock

Handset with mechanical lock function

Caregiver control with electrical lock function

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Removal of head/foot board

The plastic head and foot boards can be removed. To remove, grab the board with 2 hands and pull upward (fig.1). To fit to the bed, engage rods at the bottom of the board into the socket on the frame (Fig.2) and press until it stops.

For some patient conditions, permanently fixing the boards to the bed frame is necessary. A set of screws can provided for that purpose.

6.2 Split siderails

The MMO 6000 bed can be equipped with metal split side rails. These are positioned on the bed in compliance with safety clearances required by the regulations and to avoid the risk of jamming. They are retractable towards the outside of the bed by simple vertical action on the plastic handle on the front. An integrated soft slow motion to avoid noise and shock. Split side rails cannot be removed.

Attention in the down position, the barriers is approaching within 120 mm from the ground. However, the side rail weight does not constitute a risk of dangerous

jamming.

These sockets are designed for the accessories from the manufacturer. The use of non-approved accessories may result in increased emissions or reduced immunity of the equipment. A list of approved accessories is included in the user manual.

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7 Product description

Standard equipment

- Front exit - Split siderails folding outwardly and dampened - Variable height and electric backrest - Backrest articulation of 23 cm, designed to reduce sheer on skin of patient - Electric knee break, with manual calf section - Hand pendant with selective lockout of functions - Four support of IV pole - 4 double castor 100mm wheel directional in head - 4 double castor 100mm wheel with centralized braking system on foot - CPR function - Electric flattening of the bed with automatic height adjustment

Options : - Removable wall guard - Fixed or rotating patient helper with adjustable handle - IV pole fixed height or variable height - Infrared remote, not available in the UK or EIRE

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7.1 Dimensions Dimensions Observations Height of deck in high position 83 cm (castor Ø 100mm)

Height of deck in low position 31 cm (castor Ø 100mm)

Total lenght 214 cm

Width with 99.8 cm

Width with folding siderail 99,8 cm

Height of siderail on the deck 38 cm

Height of headboard and footboard compare to deck

45 cm Removable head and foot board

Dimension of deck 200 x 90 cm 4 removable parts

Weight of bed without mattress nor accessories

175 kg Depend of configuration

Backrest angle 70°

Legrest angle 20° On option

Thigh section angle 30° Electric version

Calf section angle -20° to+20° On option

Trendelenburg angle +10°

Reverse Trendelenburg angle - 10°

7.2 Technical specifications

MECANIC

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Safe working load 250 kg (215 kg patient, 20 kg mattress and 15 kg accessories mattress)

Basic wheels 8 wheels 100mm diameter directional wheels on head and the foot, central braking

Hydraulic shock absorber for backrest CPR

ELECTRIC Supply voltage 100-240 VCA

frequency 50-60Hz

Recommended Service ratio 10% max or 2mn continues and 18mn of rest

Output voltage of the transformer 24VCC – toroidal transformer

amperage 5,5A max per canal, 8A max total on secondary 2A max on primary

electric power 4VA idle 400 VA max full load

Electronic protection Individual in case of overload Durability of non-resettable thermal circuit breaker relays

Fuses Interne 1,25 AT

Patient control unit Linak type HL75 (selective lock out) and/or HB20 (infra-red)

Caregiver wireless control unit and lockout 3 batteries LR03 – AAA

Power supply unit Linak type CB16

Power supply wire 3x1.5 mm² PVC sleeve– interchangeable

Variable height actuator Linak type LA40 – 6000N

Front exit actuator Linak type LA31 – 3000N

Back rest actuator Linak type LA27 – 3500N

Thigh raiser actuator (as per version) Linak type LA27 – 3000N

Protective grounding class Class I

Class of protection against dust and water IPX4 – IP66 for remote HL75

Classification of the device Type B according to EN 60601-1

Backup battery In base integrated in control box

ENVIRONMENTAL CONDITIONS OF USE AND STORAGE Temperature of use From 5°C to 40°C

Temperature of storage From -10°C to 50°C

Time to rest temperature in the system after safety stop of the bed

5 hour after plugging power cord.

Humidity From 20% to 90% - to 30° without condensation

Atmospheric Pressure 700 to 1060 hPa

Maximum operating altitude 2000m

Max temperature of parts 59,8° (for electrical boxes)

Sound level 41dba

7.3 List of parts covered by ISO 60601

• Electronic box • Power cables • Hand pendant • Head and footboard • Barriers • Deck and mattress • Patient helper

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• IV pole • Castors • Brake pedals

7.4 Maintenance specification for electronic parts and actuator (LINAK)

Maintenance: valid for all products LINAK • LINAK products must be cleaned at regular intervals to remove dust and dirt, and must be inspected for any damage, wear and breakage. • LINAK products require no internal maintenance. • Only IPx6 versions are waterproof, and only IPx6 Washable versions tolerate cleaning tunnel. • LINAK products must be IPx6 Washable to be cleaned by washing tunnel. The sockets must be properly connected and equipped with O-rings. • O-rings: if required to replace one LINAK IPx6 or IPx6 washable O-ring, you must replace the complete set of O-rings. This also applies for O-rings for the fuses on the control switches. Fuse gaskets must be replaced each time the fuse is replaced. Each O-rings should be lubricated prior to fitting. (Make sure that the parts in contact with the O-rings are not damaged). Maintenance: Valid for LINAK actuators and columns • The actuators and columns should be inspected at their mountings, cables, fencing, plugs and operation. • In order to maintain pre-lubrication, it is recommended to clean the actuator when the rod is retracted. Maintenance: Valid for control boxes, manual controls and accessories • The electronic parts must be inspected at their mountings, cables, fencing and plug. • Check the connections, cables, fencing, and plugs and the proper functioning of the whole machine. (Does not apply to versions running on batteries) • Inspect the position and condition of the ventilation of external batteries, see Figure 1 Figure 1 Ventilation of external batteries: BA18 Regularly check the state of the ventilation stub. This tube (stub) allow air to pass but not water

Before commissioning: Make sure the system has been installed in accordance with this user guide. The components (actuators, columns, manual command etc.) must be connected

before powering the control box.

Make sure the compatibility of the mains voltage and that indicated on the label on the control box.

Check compatibility between the power supply and the actuators. Ensure no obstacles prevent the full operation of each function on the bed. Perform full function check following installation. The actuator should not exceed the recommended limit value indicated on the label. Follow manufacturers recommended guidelines for servicing. Failure to do so could

result in the actuator becoming damaged, thus reducing its lifetime of the product.

Unless otherwise stated on the product label, the maximum duty cycle is 10%, or 2 minutes maximum continuous use followed by 18 minutes of rest.

All actuators must be used in a suitable environment. Any known or suspected damage to components or product must be repaired/

inspected by a qualified person. Alternatively return to the manufacturer.

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Operating: If you encounter noise coming from the actuator during use, it is recommended to stop

using the bed and investigate.

If you encounter any noises or strange smells coming from the control box, immediately disconnect the bed from the mains power supply and / or batteries.

Do not use the bed if the mains or other cables on the bed are damaged. Remember to unplug the mains power cable if the bed needs to be moved.

8 Use of different product features

For your safety, before using the bed, it is essential to verify that: The mattress you intend using is compatible with the bed. The recommended mattress dimensions are 1980 x 880, mini density 35 kg/m3. Mattress maximum thickness of 15 cm for folding side rails with 3 bars and split side rails. Mattress maximum thickness of 26 cm for folding side rail 4 bars. The mental condition of the patient is compatible with the use of side rail. Ensure no obstacle or persons hinders or may hinder the movement of the side rails during use, especially when setting the low position and chair position to avoid jamming. Ensure the brakes are applied properly in the locked position if the bed does not have to be moved. NOTE: It is necessary to keep pressing the button for the entire duration of the desired movement. Exception for this is when the bed goes down and reaches a height of 12cm from the floor. At this point the bed pauses to indicate a risk of crushing if an object or bodily part is located between the bed and the floor. To continue to the extra low position release the button, then press again. This will lower the bed to the lower position. An audible signal will sound to alert the user

of the reduction of the space between the floor and the bed.

8.1 Variable height

In its lowest position, the deck is 31cm from the floor. The bed can be positioned at any height between the highest and lowest positions.

Maximum care height for the bed is 83cm (with castor dimensions 100mm)

The brake will engage automatically when it reaches its lowest position. The bed must be raised by 5cm above the lowest height (31cm + 5cm) in order to release the brakes and move the bed.

The lowest height position on the bed is recommended for patients with dementia or with high risk of falling.

Operation: The height of the bed is adjusted using the remote control.

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Press the left side of the button to go up or right side to go down to the desired height.

Warning: for irregularly monitored patients, it is advisable to leave the bed in a low position to reduce the risk of injury in case of falls. Under certain circumstances it may be necessary to prevent operation of the bed controls, therefore we recommend you use the lockout functions on the hand control.

8.2 Articulation of the bed deck

8.2.1 Electric backrest

This command allows you to adjust the angle of the backrest The electrical backrest MMO has got a special movement that reduces the lower back sliding and compression when changing position. This gives better comfort to the patient and reduces the risk of shear. The backrest angle goes from 0 to 70°. Operation: The adjustment of the backrest only occurs with the use of the hand pendant or remote control. Press the left side of the button to tilt up or the right side to go down. To operate backrest and legs section simultaneously, press the "comfort position" button.

Backrest alone

Backrest and thigh rest simultaneous move

This bed is equipped with a manual CPR function, along with a damper to assist with the descent of the backrest movement. Electrical CPR is operated by simultaneously pressing the two back rest buttons.

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8.2.2 Operating the safety flattening of the bed when the power supply is cut

The following operation should be performed when the bed is unoccupied and without mattress. The electrical backrest will become inoperative.

- Lower barriers if they are raised. - Remove a clip on the top axis of the actuator of the backrest. - Hold the backrest using the handles in the corners of the deck throughout the operation. - Pull the pin on one hand and support the bust to the horizontal with the other hand.

Setting the bed to a flat position without electrical supply

8.2.3 Operating CPR function with a patient in bed:

The following operation should be performed if the bed is occupied. The electric backrest will operate normally. - Lower the side rails if they are raised. - Hold the backrest by the handles in the corners of the deck throughout the operation. - Pull the orange handle at the central portion of each side of deck until the backrest is

completely flat. The backrest function becomes operational as soon as the handle is released.

IMPORTANT: This device should not be used as a simple backrest tilt adjustment. Improper use of CPR release mechanism may degrade the device prematurely.

Bilateral CPR handle

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8.2.4 Electrical thigh section and manual calf section

This function allows you to electronically set the thigh section and manually set the calf section. The angle of the thigh section ranges from 0° to 30°, and the calf section ranges from +/- 20° (see drawing below).

Electrical knee section alone

Electrical backrest and Knee section

Operation: to operate the tilt function for the thigh section use the remote or hand control.

Press the left button to tilt up or the right button to tilt down. This function controls the thigh section on all versions of the bed. It is possible to have both functions operating simultaneously by pressing the "comfort position" button. To operate the manual calf section in the up position, use the handle on the side of the deck and lift it to the desired position. To lower, raise the calf section slightly to release the catch, then lower in a horizontal position.

Ensure that the calf section is in low position before lowering the thigh section to avoid an inverse folding and discomfort to the patient.

8.2.5 Comfort position

This function controls the backrest and thigh rest simultaneously. This function is not possible with the manual mono-block leg section

Operation: The tilting is done by using the remote control. Press the left side of the button to tilt up or on the right side to tilt down.

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8.2.6 Storing the bed exit height into the electronic memory

This function allows you to adjust the height of the exit position to the height of each patient. This assures perfect ergonomics, reduces the effort to exit the bed and reduces the risk of falling.

Operation: At the first use of the bed by a patient, ask him/her to sit in exit position. Using the remote put the bed in the most comfortable position for the patient. Simultaneously press the two buttons on the comfort position on the remote for 5 seconds. A beep will occur when the memory is registered. Then the bed will stop at this position when raising or descending.

8.2.7 Front bed exit and Chair position - 1 button operation

The chair position allows the resident sitting. It combines the comfort and the Trendelenburg position in a continuous cycle, using only one button. If the foot board is removed, when continuing to press the button the bed will go in exit position. Operation: setting the chair position and front exit positions are carried out using the remote control. Press the comfort buttons to the maximum setting position shifts thighs, then keep pressing the same comfort button until the Trendelenburg movement puts the bed in the chair position. Continue to press the button until the complete chair position is achieved, if the footboard is not already removed, remove footboard. There is a 3 seconds pause, then if you keep pressing the button the bed will reach the floor exit position. Once in floor exit position use the height up function to aid patient standing. For the overhaul, press the back rest button until the bed is flat.

The front exit movement requires the mattress attachment on the bed frame, by 4 straps at pelvis and feet patient position

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Make sure the straps are secure and do not interfere with the movement of the side rails.

Before doing front exit, make sure you have enough space at the foot of the bed for the maneuvers.

Ensure that the flexibility of the mattress allows a perfect follow-up of the important movement of the bed deck

• Once secured to the bed by the straps, make sure that the mattress cover is

fully closed by the zip before any front exit movement.

8.2.8 Trendelenburg/Reverse Trendelenburg Position

This function should be used with the deck in flat position. The tilting of the deck without setting it back to flat will provoke a sliding of the resident downward.

The Trendelenburg function allows you to tilt the bed toward the foot of the bed. Press the right button of the Trendelenburg function until the bed reaches the angle desired. To put back to horizontal, press the left button of the Trendelenburg function. When the bed reaches the horizontal position, a 3-second stop happens. If you continue pressing the button, the opposite Trendelenburg movement begins.

A chair position can be achieved by putting the patient in the maximum comfort position then operating the Trendelenburg position.

The Trendelenburg / reverse Trendelenburg position is related to clinical indications and should be used only upon prescription. Only use the Trendelenburg/ reverse Trendelenburg function when the brakes are locked. Ensure sufficient head space around the bed to manoeuver.

8.2.9 Electric CPR Function

Electric CPR function operates the actuators to a flat position within seconds of simultaneously pressing the backrest Up and Down button. This also sets the bed to the relevant height for a cardiac massage by the caregiver.

Operation: to operate the electric CPR using the hand control. Press the Up and Down buttons simultaneously. This will set the actuators to a flat position, with the bed set to a relevant cardiac massage position. This function can be locked out on the patients hand control, but is overridden by the caregivers hand control.

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8.2.10 Under bed night light

The night light switches an LED on under the bed platform to assist the patient getting in and out of the bed at night

Operation: to operate the under bed night light is by simultaneously pressing the bed and knee lowering buttons on the hand control. To turn off the under bed light, repeat the process as above.

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8.2.11 Wall protection and position indicator (option)

The bed is equipped with 4 corner bumpers to absorb shock. The bed also incorporates a retractable visual indicator with automatic return, integral brake system serving as a position indicator to prevent the moving parts of the bed to contact the wall at the bed's angular movement. The retractable indicator stops to verify that the bed is at a suitable distance to perform a full reverse Trendelenburg of the bed (chair position) Warning: setting full Trendelenburg requires the bed to be 30cm away from wall. To retract the stop with automatic return, pushing up its engagement of the pawl. To put it back into its protective position, pull on the latch button, the stop will reposition automatically. Telescopic wall protecting buffer

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8.3 Brakes

The bed is equipped with brakes acting on the wheels in front and back of the bed.

Operation: To use the brake press on each trigger that is on the wheels. To unlock the brakes, tilt them back up with the tip of your foot.

According to the standard 60601-2-52 braking the bed is certified up to an angle of 6 ° relative to the horizontal plane on a concrete floor covered with a material of vinyl coating of 2 mm to 4 mm thick, in normal use of bed.

The bed is equipped with an automatic braking system when the bed is in the low position. Whilst in this position it is not possible to release the brakes. In order to release the brakes it requires the bed to be raised by at least 5cm above lowest height (21cm +5cm). Be mindful of possible entrapment of the foot when putting the bed in the low position as the brake pedal is automatically activated in the low position.

If the bed does not have to be moved, it is strongly advised to use the brakes to avoid potential falls when coming in or out of the bed.

Before stopping the bed in final position, be sure that nothing will prevent proper movement of the bed up, down or sideways.

Manipulation: to brake push with your foot on the braking pedal. To un-brake push up with your foot under the braking pedal

During the maintenance of the brake module, make sure that the spring of the mechanism is not damaged.

Handling is prohibited: it could slacken the spring of the brake system which can damage the mobility of the bed when the brakes of the bed are not on.

Brake lever bar

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8.4 Transferring the patient in the bed

The MMO 6000 is equipped with directional wheel on the head of the bed. This helps moving around tight corridors or on long distances with or without the patient.

Operation: If the bed has the multidirectional wheel at the head, put brakes on head wheels. This will prevent lateral move of the bed but forward and backward moves are still possible.

It is recommended to move the bed at a speed appropriate to avoid shock or damage to the element of the bed. (The bed is intended to move within the room of the patient for cleaning purpose and for patient care)

8.5 Moving the bed

In order to move the bed, proceed as follows: For small movements with the mains cable still attached to the mains power

supply, check that the power cord is not too tight and stressed.

For larger movements, unplug the power cord from the mains supply, wrap the power cord and put it between the headboard and the deck to avoid it trailing on the floor.

Check that no device or accessory is connected to the technical wall panel and cannot be damaged during movement.

Check that the IV pole and side accessories are contained within the area of the bed.

Check that the control unit for the electrical functions is properly hooked onto the bed and that its cable is not trailing on the floor.

Release the braking mechanism and put into steering position. Manoeuvre the bed using the handle on either the head or foot board

During the installation of the bed in a patient room, please check that no obstacle will hinder the movement of the bed.

Protection of the wall It is advised to respect a distance of 30 cm from the wall when installing the bed. This way when the Trendelenburg function is used the bed will not touch the wall. To help you visualize this, the wall bumper has an integrated ruler. If you remain

in the green section the bed will not touch the wall in Trendelenburg positions.

8.6 Patient restraint

The platform of the bed enables you to secure a mattress at the restraining points. These securing points are located along the edge of the bed platform panels

Using containment straps presents a risk of body injury and strangling. Using securing straps presents a risk of mattress becoming loose on the bed, with a potential of patient falling out of bed. This procedure should be carried out by the caring staff. Never fix securing straps outside the areas provided for the purpose. Never link a movable part with a stationary part of the bed.

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Deck with electrical tight movement and mechanical legs movement

Patient Strap positions

8.7 Reset procedure

An audible warning indicates that the bed is not functioning as intended. In this case you must follow this calibration procedure: press the variable height Up and Down buttons simultaneously for a minimum of 5 seconds. The audible warning indicator will stop. Then put the bed in ultra-low position (19 or 21cm – depending on castor size) and press the button for at least 3 seconds after the bed has stopped at the low position

8.8 Calibration procedure – loss of Variable height position

An audible warning indicates that the actuator on the bed has lost its position (it’s known position is not recognized) Loss of position is due to a malfunction of the control units memory or improper use of the controls and actuator movements. A loss of position should be followed by a recalibration..

8.9 Calibration procedure when overloaded

When a function is selected, the movement of the actuator stops when an overload is detected. However, it is still possible to activate another function (unless this also is overloaded). During a combined movement only the actuator which is overloaded will fail to operate.

8.10 Handling siderail:

The side rails are designed to prevent patient falls whilst in the bed. They are designed to prevent the risk of entrapment. The use of side rails for individual patients should be made by a qualified medical professional. Handling split siderail

Split side rails are assembled and are delivered fitted on the bed To raise the safety rail into position, hold the upper bar and raise it until it locks into place. To lower the safety rail, hold the grey plastic release handle in the center of the safety rail and lift vertically to release. The speed during the descent of the safety rail is reduced with the aid of a built-in damper mechanism.

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Caution: when the bed is set at the lowest position the bottom of the side rail could touch the floor. This should not cause harm to patient or caregiver.

9 Accessories

9.1 Gap filler

This accessory permits to fill the space between the side rail and the footboard The side rail can be removed even if the gap filler is in position. Each gap filler comes with a special support to fix onto the bed deck. Gap fillers are always sold in pairs (one for each side of the bed).

Operation: engage it until it clicks in position. To remove it pull the clips and pull the board.

With the gap filler in position it prevents the patient falling out of bed. Ensure the patients’ medical condition is not affected with the use of a gap filler

9.2 Head /Foot board support This device allows you to attach the opposing head or foot board for storage whilst not in use.

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9.3 Flexible holder for hand pendant

Flexible holder for hand pendant with clamping knob (the TEE59981E supports is required if you want to fix it the middle of the bed)

9.4 Siderail padding

This padding covers the side rail to avoid injury to the patient, and reduces the risk of entrapment between the side rail bars Operation: fit the cover over the top of the raised side rail, then secure in place. Note: you must remove the cover before taking away the side rails from the bed

Side rail padding for MMO ¾ folding side rails

9.5 Patient Lifting Pole

This accessory is available fixed or rotating. The handle is adjusted by simply sliding on the end of the lifting pole. The strap adjustment is made by the retractor (press the red button on the side of the retractor.) Max load for the patient lifting pole is 75kg.

9.6 IV pole

This accessory is available in either curved fixed height or straight, with 2 hooks or adjustable height with 4 hooks. The safe working load on the IV pole is 5kg max Operation: To adjust the height: unscrew the tightening ring, then adjust height, and re-tighten the ring.

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Identification label is near the hook

9.7 Remote and Hand control holder

These accessories are here to store the remote control and hand control. The remote holder has glue pad on the back to stick to most surfaces. It also has 2 holes to screw it to the wall A flexible hand control support (TEE59983G) is also available. This is fixed to the side of the bed

Note: the flexible accessory can only be used if the support TEE59983G is there for it.

10 Warranty and Installation

10.1 Warranty

The MMO bed is guaranteed for parts, labor and transport for a period of 10 years, on the condition that the bed is used in accordance with the instructions and recommendations defined by the manufacturer. Excluded from this guarantee: all electromechanical parts, engines, gas and electric actuators, remote controls and hand pendant, wheels, HPL plates). All these parts are guaranteed for 3 years. The warranty covers manufacturing defects such as welding defects, coating, assembly, operation, and abnormal structure deformation.

If spare parts are replaced during the period of guarantee, the guarantee pertaining to these parts will remain valid up until the bed guarantee expiry date.

If spare parts are replaced outside of the period of guarantee, the guarantee pertaining to these parts will be valid for a three-month period, unless the manufacturer has agreed otherwise. The manufacturer reserves the right to inspect and asses the faulty parts before validating guarantee rights. A technician team is at your service 24/7 and 365 days a year to advise you and decide on the appropriate response to any possible problem. Warranty Terms and Conditions for UK and EIRE MMO and Medstrom offer a 10-year warranty on metal frames, backed-up with a 5-year warranty on all electrical parts. This is a no-quibble warranty on the condition that a Medstrom-

Not available in the UK or IERE

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approved maintenance programme is in place utilising approved OEM parts and that the product is not subject to use beyond the manufacturer’s guidelines and normal wear and tear. For UK and EIRE customer, if no service contract is in place within the first year of purchase, the warranty will revert to two years only. WARRANTY MAY LOSE ITS VALIDITY IN THE FOLLOWING CASES: Disassembly of mechanical or electrical parts of the bed without consultation and approval of the manufacturer. Replacement parts are not supplied by the manufacturer. Work on the electrical parts or gas cylinders by un-approved personnel. Degradation of coatings or materials from shock, friction and scratches. Abnormal use of bed not following the precautions and recommendations, resulting in degradation of the bed or its environment. Using cleaning or disinfecting products unapproved by the manufacturer (see chapter 4, cleaning) Using cleaning products without respecting appropriate dilution proportions. Washing with water or using a pressure jet. Crushing or cutting the power cord or the cord of controls. Intensive use of electric bed functions beyond the recommended service factor. Use of a bed that indicates a mechanical or electrical malfunction The manufacturer, assembler or fitter may not be held responsible for the safety, reliability or the characteristics of the device unless: The electrical system within the area Accommodating the bed complies with the relevant recommendations, and the device is used in accordance with the instructions for use.

Warning: It is prohibited to make changes on the bed.

Use only spare parts approved by the manufacturer. Any item damaged must be replaced before using the bed. Disposal of the product is necessary if the essential requirements are no longer

met, especially when the product no longer has its original features. It is necessary to ensure that the bed will not be used any more. At disposal, observe the environmental standards of your country.

The manufacturer specifies that the mattress is not an element of the bed and is not part of this manual. We remind you that the mattress on the bed used to

be biocompatible according to ISO 10993-1.

10.2 Installation and commissioning

The bed is made to work in temperatures between 5°C and 40°C. The bed comes with its backrest and accessories dismantled, strapped, wrapped and packaged in protective wrapping. To carry out the installation of this product, please follow these steps; 1. Remove the protective elements and clamping (red cable ties). 2. Set backrest and accessories (as shown in the corresponding chapters) 3. Connect the power cable (located on the headboard) to the mains power supply. 4. Check that all connections are correct, the cables are not pinched and that the power cable is not too strained. 5. Perform a thorough cleaning of bed before the first use (see cleaning). 6. Upon installation of the bed in the desired location, allow for sufficient space for the different movements of the bed, this is to avoid damaging the environment or bed.

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Grid Connection: Make sure the power supply complies with current safety standards, especially as the supply voltage is 100-240 VCA + / - 10V; 50-60 Hz. The bed is equipped with an electrical protection class I (grounded). The ground connection is essential. Check that the AC outlet is properly connected to the ground. It is strongly recommended to connect the bed protected by a 30mA RCD ≤ to identify any electrical failure of the product. Precautions when use of hospital bed should be taken towards phenomena electromagnetic compatibility (EMC). The bed should be installed and put into service according to EMC requirements specified in Chapter 15. Unused connections are sealed to prevent damage from electrostatic discharge. Do not change the configuration of the bed without the permission of the manufacturer. Do not pull the mains cable to remove the plug from power outlet. Users (patients and their families) should be informed of safety rules to comply

with when using the bed.

11 After sales service

If you identify any malfunctions of the bed, call your maintenance department who will contact the MMO company agent in your country

11.1 Troubleshooting

Make first line diagnosis by following the instructions in section 14.1 If the fault has been identified and requires either spare parts or the assistance of the manufacturer or a manufacturer-approved technician: Take note of the details on the identification label, which is attached to the head of the bed before contacting the after-sales department. To order spare parts, refer to the parts diagrams and note the corresponding part references. If the fault has not been identified: Take note of the details on the identification label, which is attached to the head of the bed before contacting the after-sales department. A technician will answer your questions and inform you of the next steps.

In UK and EIRE, for service please call our UK distributor:

Medtsrom Healthcare: 2 Cygnus Court, Beverley Road, Pegasus Business Park, Castle Donington, DE74 2SA Tel: 0845 3711717 Email: [email protected] www.medstrom.co.uk

11.2 Conditions of on-site assistance and spare parts supplies

If the bed is under guarantee and the fault is within the scope of the conditions specified in chapter 9.1, the supply and shipping of the part (if the faulty part is sent back to the factory for inspection), or transport and repair expenses will be charged to MMO. If the bed is not under guarantee or if the fault is not within the scope of the conditions specified in chapter 9.1, you will be sent a quotation for the service required. Either this

http://www.medstrom.co.uk/

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estimate or an order form must be signed and returned before any after-sales services are provided. After-Sales Service (ASS) is provided by the manufacturer, or by a manufacturer-approved technician. Spare parts will be shipped from factory within 48 hours from the receipt of orders. If the part is not in stock, or if it is not included in the list of spare parts, our ASS will inform you of the delay required for supply. Caution: Our spare parts price list is reviewed on an annual basis. The manufacturer reserves the right to change the prices and references of any spare parts. Any spare parts ordered should be paid on receipt of invoice.

11.3 BED IDENTIFICATION LABEL

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12 Exploded view of the bed

Head board

Head split siderail

Foot split siderail

Foot board

Multidirectionnal Wheels Ø 100mm

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13 List of the spare parts

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FO_QA_012 MMO 6000

ID DRAWING NR PN QTY SP

1 RP5T6491 600190-5EA5 2

2 RP5T6487 600191-5EA5 2

3 RP5T7082 2

4 RP5F4750 208008-5EA5 4

5 RP5T7084 208113-5EA5 2

6 RP5F1672 147913 4

7 RP5F4785 208009 2

8 QC9D8890 9855 4

9 RP5T5927 208074-5EA5 2

10 RP5T5946 208077-5EA5 2

ASSEMBLED LEFT CAM

ASSEMBLED RIGHT CAM

PREPARED FOOT ROLLER

SUPPORT

PREPARED ELEVATION ARM

SMALL COMPENSATION

CONNECTING ROD

ASSEMBLED BRAKE PEDAL

SPIDER ROLLER

VH ARM SPINDLE

E CLIP HUB CAPS Ø14

PREPARED HEAD ROLLER

SUPPORT

SPARE PARTS

BASE

DESCRIPTION

34

2

5

1

1

6

7

8

9

10

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FO_QA_012 MMO 6000


1 RP5F7546 208078-5EA5 1

2 RP5F7565 208079-5EA5 1

3 QC9F8169 200032 2

4 QC9F8170 200033 2

5 QC9D8148 9028 2

6 QC9F6172 209535 2

7 QC9D8386 9225 2

8 RP5F6868 208048 1

9 RP5F6836 208046 1

10 QC9F3647 9570 2

11 RP5F7545 208080-5EA5 1

12 QC9F8458 207530 1

13 RP5F6837 208051 1

14 QC9F0191 42105 2

BRAKE FORK

ROLLER WHEEL Ø50 FOR SPINDLE

Ø8ZINC PLATED BRAKE WHEEL

SPINDLE

EXTERNAL E CLIPS Ø8 STEEL

SPINDLE

MOUNT. RING TRUARC RADIAL

HEXAGON NUT COVER

FLAT WASHER Z

HEAD FORK TORSION SPRING

ROLLER SUPPORT

ROLLER SUPPORT PLATE

SWIVEL CASTOR Ø100 S-BRAKE

SPARE PARTS

PREPARED HEAD ROLLER SUPPORT

DESCRIPTION

CHC SCREW

HFR NUT

4

12

10

1

11

3

13

2

5

6

7

14

98

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FO_QA_012 MMO 6000


1 RP5F7546 208078-5EA5 1

2 RP5F7565 208079-5EA5 1

3 QC9F8169 200032 2

4 QC9F8170 200033 2

5 QC9D8148 9028 2

6 QC9F6172 209535 2

7 QC9D8386 9225 2

8 RP5F6868 208048 1

9 RP5F6836 208046 1

10 QC9F3647 9570 2

11 RP5F7545 208080-5EA5 1

12 RP5T8631 207530 1

13 RP5F6837 208051 2

14 QC9F0191 42105 4EXTERNAL E CLIPS Ø8 STEEL

HEAD FORK TORSION SPRING

SPINDLE

MOUNT. RING TRUARC RADIAL

BRAKE FORK

ROLLER WHEEL Ø50 FOR SPINDLE

Ø8ZINC PLATED BRAKE WHEEL

SPINDLE

FLAT WASHER Z

SPARE PARTS

PREPARED HEAD ROLLER SUPPORT

DESCRIPTION

ROLLER SUPPORT

ROLLER SUPPORT PLATE

SWIVEL CASTOR Ø100 S-BRAKE

CHC SCREW

HFR NUT

HEXAGON NUT COVER

4

12

10

1

11

3

13

2

5

6

7

14

98

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FO_QA_012 MMO 6000


1 RP5T6560 41600-5EA5 1 #REF!

2 RP5T6948 1

3 QC9D2460 12992 2 10,70 €

4 RP5T6946 1

5 QC9T2720 141290 1 97,50 €

6 QC9T7283 42005 1 #REF!

ASSEMBLED THIGH REST

SPARE PARTS

LEG REST

DESCRIPTION

TELESCOPIC LIFT-UP FITTING

ELECTRIC SCREW LIFTING JACK

BUNCHED CONDUCTOR

ACTUATOR POWER CABLE

4

3

61

2

5

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FO_QA_012 MMO 6000


1 RP5T6908 600145

2 RP5T6909 600144

3 RP5S9843

4 RP5S9555 41850-5ET5

5 RP5D9945 40184

6 RP5T6792

7 RP5D9947 40182

8 RP5D9960 40186

1/2 PREP LEFT HEAD BARRIER

SPARE PARTS

HEAD HALF-BARRIER

DESCRIPTION

1/2 PREP RIGHT HEAD BARRIER

ASSEMBLED SINGLE ARM

LOCKING COMMAND

REAR HUB CAP

TUBE PIROGUE

4

3

6

1

2

58

7

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FO_QA_012 MMO 6000


1 RP5T6914 600142

2 RP5T7440 600143

3 RP5S9843

4 RP5S9555 41850-5ET5

5 RP5D9945 40184

6 RP5T7359

7 RP5D9947 40182

8 RP5D9960 40186

1/2 PREP LEFT FOOT BARRIER

SPARE PARTS

FOOT HALF-BARRIER

DESCRIPTION

REAR HUB CAP

1/2 PREP RIGHT FOOT BARRIER

ASSEMBLED SINGLE ARM

LOCKING COMMAND

TUBE PIROGUE

43

6

1

2

5

8

7

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FO_QA_012 MMO 6000


1 RP5T4645 1

2 QC9S9825 39137 1

3 RP5T6738 41890-5EA5 1

4 RP5T7236 41893-5EA5 1

HYDRAULIC SHOCK ABSORBER C

220 mm

ASSEMBLED COUNTER-ROD

ASSEMBLED BACKREST

SPARE PARTS

BACKREST

DESCRIPTION

3

4

1

2

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FO_QA_012 MMO 6000


1 RP5T6501 41830-5EA5 1

2 RP5T6510 41820-5EA5 1

3 RP5T6915 600143 1

4 RP5T6914 600142 1

5 RP5D9363 39108 2

6 AT5D6557 19291 4

7 RP5D9380 39103 4

8 RP5D9799 39106 2RIGHT CORNER FITTING

STOP FASTENING CLIPS

SPARE PARTS

FRAME

DESCRIPTION

BED EXTENTION FRAME

CENTRAL SECTION ASSY

RIGHT FOOT SPLIT SIDERAIL

LEFT CORNER FITTING

STOP Ø 100

LEFT FOOT SPLIT SIDERAIL

1

2

3

4

6

5

7

8

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FO_QA_012 MMO 6000


1 RP5T7072 600137 1

2 RP5T7073 600138 1

3 RP5T7248 1

4 RP5T7249 1

5 RP5F7702 250727 2

6 QC9F8898 67304 18

FIX SECTION SLEEP DECK

MATTRESS RETAINER

RUBBER BUNG

PIECES DETACHEES

SPARE PARTS

SLEEP DECK

DESCRIPTION

BACKREST SLEEP DECK

2

4

1

5

3

6

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MAINTENANCE GUIDE FOR MEDICAL BEDS

Levels 1 & 2

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14 Maintenance guide for medical beds Levels 1 & 2

14.1 Manufacturer’s commitment:

Warranty:

Furniture: 10 years guaranteed against defects or failure under normal use conditions. Mattresses: guaranteed 2 years Electromechanical parts (engines, gas and electric actuators, remote controls, wheel of medical beds, thermoformed plates) ) see Warranty paragraph 10

HOTLINE 0811-900-035 a specialized staff is ready for you 24/7 - 365/365 days

14.2 Organization of services:

Spare parts: We have a stock of spare parts for all of our products based on our factory in Vitre, 35500, France. We provide quote for spare parts in 48h.

We send out your order within 48h by international parcel services.

Availability of spare parts Minimum 10 years after the end of commercialization for Medical beds

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Personal notes

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14.3 Preventive maintenance

Only authorized trained staff may perform the maintenance tasks described in this chapter. Unauthorized or untrained staff may risk injury or electrical shock. Before carrying out any necessary maintenance tasks ensure the bed is disconnected from the mains power supply and that lock-out functions are disabled. We recommend that the MMO 5000/ MMO 5000+ bed has an annual preventative maintenance in order to maintain optimum function efficiency and operation safety of the bed. This procedure helps to eliminate any risk of alteration of performance and prolonged product downtime. Preventative maintenance involves carrying out a visual and functional check. We strongly advise you to carry out this check in the following cases: 1st product operational use. Following a long idle period. After having carried out a corrective maintenance task involving electrical or mechanical parts of the bed. Annual maintenance under normal conditions of use. The checklist provided in the present manual will enable you to optimise maintenance operations and ensure the traceability of all of your beds. If faulty components affecting bed safety and performance are identified, the bed must not be used.

CAUTION: The replacement of parts from suppliers other than the manufacturer is prohibited. Failure to follow this may result in cancellation of the guarantee and/or could potentially cause injury to patient or caregiver.

To allow you to follow the preventive maintenance schedule, a label defining the date of the next inspection is affixed to the frame besides the identification label. During an inspection, see the date of your next annual review on this label. All damaged components must be changed prior to use

BED MAINTENANCE CONTRACT Preventative inspections may be carried out by the manufacturer, or by a manufacturer-approved technician. A contract signed by both parties is required for this procedure. For further information concerning the maintenance contract, please contact the MMO after-sales service.

AFTERSALE SERVICE MMO :

MMO SAS 24 ROUTE DE BEAUVAIS 35501 VITRE FRANCE Tel: +33 (0)2 99 75 04 50 – Fax: +33 (0)2 99 74 65 71 OR OUR HOTLINE IN FRANCE +33 (0)811 900 035

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Check List Medical Bed

Identification of medical device Hospital

Category: MEDICAL BED

Brand/Model/Type: MMO 5000

Serial n° : Department / Location:

Date of Manufacture:

Qualitative aspects NA YES NO

Operational and visual checks

OVERALL CONDITION

Availability of user manual and technical manual

Good overall condition (bed ends, protecting buffers, bed platforms, castors…)

Acceptable level of corrosion with regard to user service requirements

Satisfactory condition of identification tags / labels / screen-printing

The side rails fitted are designed for this particular bed and meet the operational requirements

MECHANICAL FEATURES

Absence of noise annoyance (creaking, lubrication..)

Torque checks (nuts and bolts, pins, pivots, clips...)

Satisfactory condition of lifting pole (attachment and strap)

Satisfactory condition of mechanical cables

Satisfactory condition of bed platform

Functionality of leg raiser

Functionality of calf section

Correct position and correct attachment of side rails

Functionality of side rail locking systems

Functionality of integral bed length extension

Functionality of castors (swivelling, rolling, steering)

Functionality of bed immobilisation (castor brakes…)

ELECTRICAL FEATURES

Functionality of back rest

Functionality of thigh raiser

Functionality of comfort position

Functionality of calf section

Functionality of Trendelenburg / reverse Trendelenburg

Functionality of Ergo-Chair position

Functionality of medical care position

Functionality of shock position

Satisfactory condition of electrical cables (no cuts, not pinched…)

Satisfactory condition of electrical parts (power supply, motors, units, external sensors)

Satisfactory condition of hydraulic and pneumatic parts (cylinders, shock absorbers…)

Satisfactory condition of unit controls, display functions, LEDs

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Safety check NA YES NO

Operational function lockout

Functionality of emergency lowering function (CPR)

Satisfactory load resistance of the motors

Correct operation of visual and sound alarms

Quantitative aspects NA YES NO

Satisfactory battery-operation of bed

Check to ensure the height of the side rail at the top of the non-compressed mattress complies with the standard in force, which is 22cms

AMPLITUDE OF MOVEMENTS

Back rest : Maximum angle according to manufacturer’s specifications

Thigh raiser: Maximum angle according to manufacturer’s specifications

Maximum height: according to manufacturer’s specifications

Minimum height = according to manufacturer’s specifications

Comments

Conclusion YES NO

Operational

Action required (refer to comments)

Recommended date of next inspection:

Operator

Name:

Hospital

Date :

Signature :

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15 Servicing

Only authorized trained staff may perform the maintenance tasks described in this chapter.

Unauthorized or untrained staff risk injury or electrical shock. Before carrying out the necessary maintenance tasks, and after having put the bed into the required position, if the bed is equipped with backup batteries, it must be unplugged from its power source and all its electrical functions must be locked-

out.

15.1 First Level diagnosis

The most common types of fault are given below to help reduce troubleshooting time. A/Fault : None of the bed functions are operational The green LED on the power supply unit is illuminated Steps 5 to 9

Steps 1 to 4 1 Check to ensure the bed is connected to the mains 2 Check the power supply wire to ensure it is not crushed or cut, and that it is connected to the power supply unit. 3 Check to ensure the wall socket is powered, or plug the bed into a different socket 4 Replace the power supply unit 5 Check the functions have not been locked out (lock open) on the carer control unit 6 Use both control units (patient / carer) to test function availability (test a common function such as variable height).The bed operates via the carer control unit

Steps 7 & 8

Step 9

7 Check the condition of the patient control unit power supply wire and check that it is connected to the power supply unit. 8 Disconnect the patient control unit and try using a different one (cf wiring diagram). 9. Replace the control unit

B/ Fault : The articulated section adjustment function does not work The other functions are operational (variable height and Trendelenburg/Reverse Trendelenburg Controls) NO → See above

The back rest movement function does not work: The electric motor of the back rest functions, but the back rest does not move. YES → Steps 3 and 4 1 Check to ensure the manual release function is activated and that the control housing is not jammed. 2 Release the back rest and lift or lower it manually to engage the coupling. One of the articulated sections does not work: 3 Check to ensure the function in question has not been locked out (lock open) 4 Test the function response on both control units (patient / carer)

- Yes

No

- Yes

No

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The bed operates via the carer control unit NO → Step 7 YES → Steps 5 and 6

5 Check the condition of the patient control unit power supply wire and check that it is connected to the power supply unit.

6 Disconnect the patient control unit and try using a different one (refer to wiring diagram). Replace the patient control unit The bed operates normally

IF No ↓ 7. Replace the power supply unit. Invert 2 motor inputs on the power supply unit (connections marked 2, 3 or 4 on the wiring diagram).The faulty function is now operational and the function corresponding to the inverted input does not work. Replace the power supply unit. IF No ↓ 8. Replace the motor corresponding to the faulty function. C/ Fault : The variable height function does not work (no intermittent sound signal)

The other functions are operational No → See chapter 8.8, p34

Yes ↓

The electrical function of the bed functions but the bed does not go up or down YES → step

4 No ↓

CAUTION: In this case, do not manipulate the Trendelenburg, reverse Trendelenburg, the shock position or the Ergo-Chair position functions. 1 Check to ensure the function has not been locked out (lock closed) 2 Check the power supply wire to ensure it is correctly connected to the power supply unit (connection marked 1) 3 Invert 2 motor inputs on the power supply unit (connections marked 1 and 5). The faulty function is now operational and the function corresponding to the inverted input does not work. No ↓ YES → Replace the power supply unit

4. Replace the variable height motor D/Fault : the CPR function does not work

1. Check that no object is preventing the movement of the back rest or the handle

Note: the CPR function is a gas dampener. Some pressure is needed on the back rest for it to come down, especially if the bed is empty. 2. Check that the CPR function cable are not blocked or broken

E/ The bed is difficult to move and the wheels does not work (no intermittent sound signal). 1. Check that the brakes are disengaged (foot pedals in high position). 2. Check that the wheels are not clogged or blocked by an obstacle. 3. Or replace the defective wheels or brake F/ Fault : bed emit sound signal Analyzing the sound signal

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Fatal Error (error detected in one or more cylinders): Simultaneously press the 2 buttons on 2nd line of the hand pendant. An intermittent signal sounds, maintain pressure until disappearance of the signal. Replace the high maximum position and then bed down in the down position. Complete full Trendelenburg and then reverse Trendelenburg

Thermal Default (temperature difference between the reference temperature and the current temperature): plug bed in to the power socket for 5 hours without any movement of the bed as this process is reset every time the hand control is activated. It is possible to reprogram without waiting 5 hours (to be performed with software by a service center technician). Battery charge level

Battery charge level (low battery charge warning): Leave the bed connected to recharge the battery.

15.2 Second Level – wiring diagram

Only authorized trained staff may perform the maintenance tasks described in this chapter. Unauthorized or untrained staff risk injury or electrical shock. Before performing any troubleshooting tasks and after having put the bed into the required position, if the bed is equipped with backup batteries, it must be unplugged from the mains power supply and all of its electrical functions must be locked-out. All faulty electrical components must be replaced. Do not perform any repairs inside the motor housing, the control units or the power supply unit. Do not make any alterations to any of the electrical assembly or components. Before replacement, check to ensure the spare part reference corresponds to that of the original part. Spare parts must be supplied by the manufacturer only. Any parts supplied, other than the manufacturer may jeopardise the safety and performance of the bed. The manufacturer cannot be held responsible if modifications are made to the original features of the bed, or if non-approved parts are used.

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The cable connectors must be fitted to the corresponding port to prevent abnormal operation or damage to the bed. WIRING DIAGRAM This diagram is shown on the cover of the power supply unit. The wires are fitted with numbered rings so that their position may be identified on the terminal block.

Caution: Unused connections must be blocked to avoid electrical risks resulting

from electrostatic discharge or infiltration.

FO_QA_012 MMO 6000

PN 9933 207515 207514 92817 92818 207368 42002

PRICE

PN 207796 42006 21543 21542 42010 21540 21541

PRICE

PN 150928 141290 42003 42005 207513

PRICE

SPARE PARTS

WIRING DIAGRAM

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15.2.1 Replacement of the patient hand pendant(refer to wiring diagram)

Raise the bed to the maximum height position (if possible), then unplug the bed from the power supply.

Remove the central section of the bed platform to access the power supply unit. Remove the retaining clip at the top of the power supply unit. Disconnect the patient hand control unit from the power supply unit by pulling firmly

on the cable.

Lubricate the ring area of the connector to facilitate positioning and re-connect it. Insert the retaining clip back into place and fit a new collar. Plug the bed back into its power supply and check functionality.

15.2.2 Replacing the control box

1. Raise the bed to the maximum height position (if possible) and unplug the bed. 2. Remove the central section of the bed platform to access the power supply unit 3. Remove the retaining clip underneath the control box. 4. Disconnect all connections. 5. Unscrew the two fixing points on the control box, then remove. 6. Position the new control box and reconnect all cables to set ports. 7. Refit the retaining clip on the connectors. 8. Screw the 2 fixing points of the control box. 9. Reconnect the bed to the power supply, then check functionality.

15.2.3 Replacing the electric actuators

Backrest actuator

1. Raise the bed to the maximum height position (if possible) and unplug the bed. Lock out all of the electrical functions except for the back rest section. 2. Remove the back rest section of the bed platform to access the actuator. 3. Disconnect the motor power cable. 4. Slide back the retainer hatch to access the manual control cable connection and disconnect the cable ends. 5. Remove the left C-clip from the clevis pin to the damper. Slide the pin to remove the damper. Repeat the procedure on the opposite end. 6. Put the new motor into position and re-connect the clevis pins. 7. Put the C-clip back into position and check to ensure they rotate freely. 8. Slide back the hatch on the motor and put the cable back into place. 9. Slide the hatch into the closed position and lock. 10. Connect the actuator power cable to the control box (ensure O-ring seal is fitted prior to connecting). 11. Check electrical and manual functionality of the back rest. Thigh section actuator

1. Raise the bed to the maximum height position (if possible) and unplug the bed. Lock out all of the electrical functions except for the thigh section 2. Remove the thigh section of the bed platform to access the actuator . 3. Disconnect the actuator. 4. Remove one of the two C-clips from the clevis pin. Slide the pin to remove one end of the actuator. Repeat the process of the opposite end. 5. Put the new actuator into position and re-connect the clevis pins. 6. Put the C-clips back into position and check to ensure they rotate freely. 7. Plug actuator cable back into position 8. Connect the bed back into its power supply and check functionality Replacing the variable height motor

+

+ +

+

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Caution: This procedure requires special precautions as the variable height motor connects the main frame assembly to the bed platform. If the bed is set at a raised position, support the bed platform before disconnecting the actuator.

1. Remove all the sections from the bed platform. 2. Raise the bed to the maximum height position (if possible), then raise the back rest section to the highest position. 3. Support both ends of the bed platform (alternatively put the bed into the lowest possible position). 4. Unplug the bed from the power supply. 5. Unplug the actuator. 6. Disconnect the motor attachment bolts (16 wrench and 17 ratchet). 7 Reverse the procedure to fit the replacement actuator 8. Adjust the length of the actuator with selecting the variable height function on the hand control before putting the second screw in position 9. Fasten the bolt. 10. Perform a full raise and lower function on the bed

15.2.4 Replacing the castors

1. Raise the bed to its highest position and unplug the bed from the power supply. 2. Securely support the underside of the bed using a jack (or similar supporting product) and check the stability. 3. Lower the bed onto the jack to disengage the castors from the ground. 4. Unplug the bed from the power supply 5. Unscrew the castor with a hex key. 6. Fit the new castor after checking it can rotate freely 7. Perform a full movement test, including tracking and braking

15.2.5 Replacing the CPR cable

1. Raise the bed to its highest position and unplug the bed from the power supply. 2. Remove the back rest section of the bed platform. 3. Slide the retaining hatch to access and remove the manual control cable. 4. Tighten the cable sheath stop to full torque to slacken the cable, loosen the cable clamp (mark 6) and remove the cable. 5. Thread the new cable into the sheath, and fit the cable end into the appropriate point on the actuator. 6. Thread the other end of the cable into the cable clamp, tighten and adjust the tension using the sheath stop and the locknut. 7. Check electrical and manual functionality of the back rest.

15.2.6 Replacing a backup battery

1. Raise the bed to its highest position and unplug the bed from the power supply. 2. Remove the back rest section of the bed platform to access the battery. 3. Unlock the power cord of the battery and unplug it from the control box. 4. Unscrew the two screws securing the support plate and remove the battery. 5. Remove the battery fixing screws on the plate. 6. Replace the battery 7. Repeat the reverse procedure to fit the replacement battery 8. Check the electrical functionality without connecting power to the bed , then reconnect the power supply.

+ +

+

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16 Data

16.1 Electromagnetic compatibility

Precautions for use of electro-medical equipment must be taken vis-à-vis the phenomena of electromagnetic compatibility (EMC). Electro-medical equipment must be installed and put into service according to the EMC recommendations attached in the technical manual. Interference may be caused by the proximity of communications equipment and mobile phones. If equipment or a professional communication system must be used in a medical area or must be connected to public low-voltage power supply, the accompanying documentation must include the following warning message: Equipment or system is under the responsibility of qualified staff. Equipment or system can be the source of radio interference or cause malfunction of other equipment located in the immediate vicinity. Some installation precautions may be necessary such as moving equipment or installation in a protected enclosure.

Manufacturer’s guide and declaration- electromagnetic emission

The MMO 6000 bed is to be used in the electromagnetic environment described below. The user must ensure that it is used in this environment

Emissions test Compliance Electromagnetic Environment- Guide

Emissions RF CISPR

11 Group 1

The medical bed uses radio-magnetic energy only for its internal function, because of this, its RF emission are very weak and not likely to cause any interference to nearby electromagnetic equipment.

Emissions RF CISPR

11 Class B

The MMO 6000 bed can be used in any premises (other than domestic premises which run on low electrical voltages).

Harmonic emissions EN 61000-3-2

Class A

Voltage Fluctuations/ Flicker EN 61000-3-3 Applicable

Manufacturer’s guide and declaration- electromagnetic immunity

MMO 5000 medical bed is designed to be used in the electronic environment specified below. The user must ensure that it is used in accordance to these guidelines

Immunity test

CEI 60601 Security level

level of compliance

Electromagnetic environment guide

Electrostatic

discharge EN 6 1000-4-2

± 6 kV on contact ± 8 kV in the air

± 6 kV on contact ± 8 kV in the air

The floor should be wood, concrete or tiled. If the floor is

covered with a synthetic material relative humidity

should be at least 30%

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Rapid transient burst EN 61 000-4-4

± 2 kV for the supply lines ± 1 kV for

input/output

± 2 kV for the supply lines ± 1 kV for

input/output

The quality of the main supply should be that of a typical

commercial or hospital environment.

Voltage

impact 61

000-4-5

Differential mode ± 1 kV

Common mode±2kV

Differential mode ± 1 kV

Common mode ± 2kV



Sags, short power cuts, variations in the voltage supply EN 61 000-4-11

<5% UT –for 10 ms

40% UT –for 100 ms

70% UT- for 500 ms

<5%UT- for 5 s

<5% UT –for 10 ms

40% UT –for 100 ms

70% FOR 500 ms

<5%UT-for 5 s



If the user of the bed wants to continue operating during a

power cut, it is recommended that the bed be powered by an

uninterruptible power supply or a battery.

Magnetic field at network frequency (50/60 Hz)

3 A/m 3 A/m The magnetic field at network frequency should be at a level that is typical for a commercial

hospital environment.

Note : UT IS THE NOMINAL VALUE OR THE VOLTAGE SUPPLY APPLIED DURING TEST.

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MMO6000 medical bed is designed to be used in the electronic environment specified below. The user must ensure it is used in accordance to these guidelines

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Recommended separation distances between portable Radio Frequency communications equipment and mobile equipment

The hospital bed is intended for use in an electromagnetic environment In which radiated RF disturbances are controlled. Users of hospital bed can help prevent electromagnetic interference by maintaining a minimum distance between the bed and RF communications equipment (transmitters) and the hospital bed as recommended below, according to the maximum output power equipment communication.

Maximum strength of emitter in

W

Distance of separation according to the frequency in m

150 kHz 80 MHz 80 MHz 800 MHz 800 MHz 2,5 GHz d = 1,17 d = 1,17 d = 2,33

0,01 0,12 0,12 0,23 0,1 0,37 0,37 0,74 1 1,17 1,17 2,33

10 3,70 3,70 7,37 100 11,70 11,7 23,3

For transmitters whose maximum output power not listed above, the recommended separation distance d in meters (m) can be determined using the equation applicable to the frequency of the transmitter, where P is the maximum output power of the transmitter in watts (W) assigned by the transmitter manufacturer Note 1 80 MHz and 800 MHz, the separation distance given in the higher frequency band applies. Note 2 These guidelines may not apply in all situations. the propagation Electromagnetic waves is affected by absorption and reflection from structures, objects and people.

16.2 Disposal at end of product life

Please dispose of the product according to your local authority regulations

16.3 Earthing

In healthcare facilities, caregivers and patients are often faced with the presence of leakage currents who in medical facilities. These currents are due to potential differences that develop between the switchgear and the metal parts present in the premises for medical use or a faulty connection to earth. The MMO bed is provided with an equipotential terminal attached to the metal mass of the bed and for connecting, via an electrical socket of the building if the latter is equipped, It is recommended to use the ground to avoid the risk of electric shock.

16.4 Life of the device

The lifetime of the bed is very dependent on its use, but can be estimated at fifteen years. It is highly recommended to regularly perform maintenance operations described in the manual in order to maintain product safety standard and ensure the integrity of users.

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17 Manufacturer’s detail

SOCIETE MMO 24, Route de Beauvais BP 90148 35501 VITRE Cedex France

Tél. : +33(0)2 99 75 04 50 – Fax : +33(0)2 99 74 65 71

For further information relating to technical characteristics, maintenance or After Sales Service, please consult the bed’s technical manual available on request from MMO. UK DISTRIBUTOR AND AFTER SALE SERVICE: MEDSTROM HEALTHCARE 2 Cygnus Court, Beverley Road, Pegasus Business Park, Castle Donington, DE74 2SA Tel: 0845 3711717 Email: [email protected] www.medstrom.co.uk

mmo 6000 - joerns.nl · 8.2 articulation of the bed deck 8.2.1 electric backrest this command...

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