USER'S MANUAL ALDRYS EVOLUTION II BED
Contents
1. Compliant The medical bed see references in contents has not been designed for connection to other CISPR 14 1 equipment Manufacturer s declaration and guide electromagnetic immunity The medical bed see references in contents has been designed for use in the electromagnetic environment specified below The user should ensure that it is used in such an environment CEI 60601 Compliance level Electromagnetic environment Guide L Immunity test Severity level Electrostatic discharge 6 kV contact 6 kV contact Floors should be wood concrete or ceramic tile If floors are covered with EN 61000 4 2 8 kV air 8 kV air synthetic material the relative humidity should be at least 30 96 Electrical fast transients 2 kV for feeders 2 kV for feeders The quality of the main power supply must be the same as for a typical EN 61000 4 4 1 KV for input output lines commercial or hospital environment 1 kV for input output lines Surges Differential mode 1 kV Differential model 1 kV The quality of the main power supply must be the same as for a typical EN 61000 4 5 commercial or hospital environment Common mode 2 kV Voltage dips short 596 Ur for 10 ms lt 5 Ur for 10 ms The quality of the main power supply must be the same as for a typical interruptions and voltage 40 U for 100 ms 40 U for 100 ms commercial or hospital environment variations d d EN 61000 4 11 If the user of the medical bed see r2. OF ACCESSORIES Lifting pole A 243 00 A576 00 75Kg Aldrys epoxy folding rails Aldrys chromed folding rails Wall stop IV stand JA1700 8 KG 8 Kg Telescopic IV stand A8400 _ 8Kg CCS Bed base extension Handle support Only accessories and boards supplied by MEDICATLANTIC guarantee safe A use gt Compatibility of the mattress Features compatible mattresses Aldrys Evolution Bed Minimum width 86 cm high resilient foam with a density of 34kg m IAL3L minimum height 14cm mini and 15 to 17cm maxi y Incompatibles mattresses may create HAZARDS 3 4 SETTING UP THE ACCESSORIES Angled lifting pole The lifting pole is intended to help the patient lift him herself up and change position in the bed It is not meant to help with transferring Fit the angled lifting pole into the slots on each side of the head end of the bed base until the tab is engaged and then put the washer and nut in place gt Wall stop The wall stop A274 00 can be mounted on the cross member of the head end of the base Remove the cross member plug and insert the stop pin in the hole of the cross member P EJ D a2 15 06 2011 7128 IAL3L 07 08 11 MEDICATLANTIC gt Folding side rail Assemble the folding side rail in the direction shown by the photo 2 Leave a space of 0 to 6 cm maximum at the head of the bed even if the board is dismantled 3 Tighten the Rondo screws of the grip jaws
3. Slatted leg rest x Bed r Footboard base A CPR handles Headboard Angled lifting pole slots IV stand slots gt A Os Castors 75 Base and cross braces D Manual crank or electric folding leg rest depending on version MEDICATLANTIC recommends the use of a patient lift or a dining table bases with less than 120 mm high Passing the patient lift under the Passing the overbed table under the Aldrys Evolution bed Aldrys Evolution bed 15 06 2011 13 28 IAL3L 07 08 11 MEDICATLANTIC 4 3 TECHNICAL CHARACTERISTICS gt Electrical characteristics Bed code Class II double insulation TF ILI I AL XP XS L 07 08 11 Current type Protection level against liquid penetration P 54 230V 50Hz FACTEU SERVICE 10 max 2min T8rsi Frequency PUISSANCE ABSORBEE 200 VA Voltage Maximum Absorbed power operating time Protection level against electric shocks type B gt Electrical data TYPE de VOLTAGE FREQUENCY LA 27 Back rest jack 24V DC CPR Jack optional Operating time 2 minutes of continuous use followed by 18 minutes down time The type and gauge of mains fuse F 1AT Weight Normal load in use 170 kg Patient 135 kg Mattress 20kg Accessories 15kg Bed version electric folding leg rest without boards 89 5 kg Bed version manual crank leg rest without bo
4. on the bed base i Maxi 4 cm HEAD end FOOT end If the side rail is poorly positioned user safety may be endangered or a malfunctioning may occur The side rails must not be used when the patient is a child or if s he is too small gt To lower the side rail 1 Take the side rail by the top rail Pull on the locking button 15 06 2011 8 28 IAL3L 07 08 11 MEDICATLANTIC gt Toraise the side rail 1 Take the side rail by the top rail and lift Check that the side rail is locked by trying to fold it without using the release pin Precaution for use There must be at least 220 mm between the top of the side rail and uncompressed mattress surface gt Full lenght wooden side rails gt Toraise the side rail D Lift the top rail with two hands until it locks 2 Check if it is well under way gt To lower the side rail D Lift the top rail with one hand 2 Press the indexing pin with the other hand 3 Accompany the descent of the side rail Repeat stages to for the other side 15 06 2011 9 28 IAL3L 07 08 11 MEDICATLANTIC 3 5 INSTRUCTIONS FOR DISMANTLING THE MOTORS AN Disconnect the 230 volts connection before dismantling e Dismantle when the bed is empty or in the side position f dismantling in any other position keep a firm hold of the moving parts to avoid any shearing e Unplug the motor leads unblock the motor clips
5. 15 06 2011 18 28 IAL3L 07 08 11 MEDICATLANTIC 10 V m transmitter manufacturer and d the recommended separation distance in metres m 800 MHz to 2 GHz The field strengths transmitted by fixed RF transmitters determined by an electromagnetic measurement of the site must be less than the conformity level in each range of frequencies a Disturbances can occur near devices marked with this symbol Note 1 At80 MHz and 800 MHz the upper frequency range applies Note 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people Field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land mobile radios amateur radio AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy To assess the electromagnetic environment due to fixed RF transmitters an electromagnetic site survey should be considered If the measured field strength in the location in which the medical bed see references in contents is used exceeds the applicable RF compliance level above the AccuGuide Monitor should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as re orienting or relocating the medical bed Over the frequency range 150 kHz to 80 MHz field strengths should be less than 3 V m Recommended separat
6. al beds will be inspected by trained technical or biomedical staff by taking account of the normal conditions for use specified in the user s manual on a bed equipped with specific safety rails The bed must be available for carrying out a full quality inspection at least once a year but also on specific request after curative maintenance on performances which could have been affected by the repairs However to save time this may be carried out at the same time as preventive maintenance In this case it is not worth carrying out a new inspection of performances that have already been checked With external test devices to the medical bed compatible with the performances claimed by referring to the user s manual if necessary 5 1 MAINTENANCE RECOMMENDATIONS FOR PREVENTIVE MAINTENANCE 15 06 2011 19 28 IAL3L 07 08 11 MEDICATLANTIC Preventive maintenance should be carried out in accordance with our specifications and at least once a year by the organisation or person who installed the bed Between two maintenance sessions and at least once a year the following should be carried out Verification that the electrical leads are connected all along the metal jambs to prevent shearing of these leads when the variable height is being activated Verification that all of the electrical leads and plugs are in good condition Replacement if there is the slightest alteration wear shearing damage etc Verificatio
7. and remove them from the securing seals e Putthe motors back in place and put in the same direction as at the beginning 3 Clip 3 6 FLATTENING THE BACK REST ON THE BED In the event of a power cut or failure flatten the back rest as follows a Disconnect the power supply b Dismantle the headboard and wooden side rail if necessary c Stand at the head of the bed and take hold of the back rest handle with one hand Push or lift to compensate the pressure exerted by the patient and unhook the clipG by the connecting rod with the other hand The back rest jack will then pivot downwards d Put the headboard back gt To exchange the jack unplug the electric lead from the motor and remove clips and Q 15 06 2011 10 28 IAL3L 07 08 11 MEDICATLANTIC Emergency flattening of the back rest optional can be used in the event of a power cut Activate one of the two handles on the back rest while lowering the back rest with the other hand If the handle is released the chest rest will stop moving Clutch release handle ELECTRICAL CONNECTION DIAGRAM Button for manual leg rest version or leg rest Back rest jack jack for electric version Variable height jack EE CN 4 CONDITIONS FOR USE 15 06 2011 11 28 IAL3L 07 08 11 MEDICATLANTIC The bed must be plugged into a dedicated socket When use of an adaptor extension lead or connection plug proves necessary you must chec
8. ards 85 5 kg zy 41 5 kg H ad end Dod Be MERECE TEE EU TTD 23 kg Foot end bed base version electric folding leg rest 0 25 kg Foot end bed base version manual crank leg rest 0 21 kg 15 06 2011 14 28 IAL3L 07 08 11 MEDICATLANTIC gt Dimensions ut J 3 Castor with 75 4 4 USE Carry out a test cycle when the bed is empty to familiarise yourself with the bed functions Version with electric folding leg rest Version with manual leg rest Lifting and lowering of back rest Lifting and lowering of variable height Lifting and lowering of electric folding Simultaneous lowering and lifting of back rest and folding HLWO 4 026 in i 15 06 2011 15 28 IAL3L 07 08 11 MEDICATLANTIC Key to lock a function KEY IN VERTICAL POSITION TURN THE KEY SLIGHTLY TO THE THE FUNCTION IS RIGHT TO LOCK THE FUNCTION UNLOCKED Manual crank leg rest To lift lift the leg rest using the wire handle at the end To lower lightly relieve the leg rest with one hand to release the catch and lower the leg rest Folding Memory folding keeps a position of the tibia section horizontal when the jack is activated upwards To use this function the crank catch must be engaged Folding without memory t
9. asured from the top of the barrier to the uncompressed mattress surface excluding therapeutic mattresses is more than or equal to 220 mm complies with the standard in force 2 Locking of operational functions s of operational functions Inactivation of variable height control pedals Cardio Pulmonary Check that the headboard extracts or Resuscitation CPR retracts properly in an emergency emergency flattening of the Check that the chest rest emergency back rest flattening function works properly Withstands jack load well Pf a Visual and sound alarms in good working order 4 Quantitative aspects Bed functions Bed functions properly using the battery using the battery Check the scale of movements Bea functions propery using the tate LL Maximum angle when Pre icd angle of specifications claimed by the manufacturer x Maximum height Maximum wn of specifications claimed by the manufacturer 20 mm Minimum height Minimum height of specifications claimed by the manufacturer 20 mm 15 06 2011 22 28 IAL3L 07 08 11 MEDICATLANTIC Comments YES Operational is the safety of the patient carers and technical staff at risk DEM Plan of action see comments 3 LL Recommended date of next quality inspection OPERATOR NAME Establishment DAE Signature S 1 Not Applicable 2 If the height measured does not comply with the standard the health manager res
10. d B C 5 Putthe bed into the low position and unplug the electric lead of the variable height motor A Take out the pins connecting the bed base cross brace and lift the frame of the half bed base E The base is ready to be moved or transported As B Rondo screws Clip Pin a E 15 06 2011 5 28 IAL3L 07 08 11 MEDICATLANTIC p gt Assembling the Aldrys Evolution bed for divisible bed base Place the base with the cross brace in the braked position 2 Position the head half of the bed base on the cross brace and secure the 2 pins Q B 3 Take out the power lead on the head end above the cross member secure it on the structure using the clip and plug into the mains F 4 Take out the electric lead s of the motors by passing them as shown on photo G and connect it them on to the variable height jack G A Test that the equipment functions properly using the handset See the electric connection diagram 5 Position the bed in its highest position 6 Assemble both half bed bases Fully screw in the 2 Rondo screws H B 7 Put the clip between the two bed bases 8 Plug in the electric lead of the leg rest motor A 9 Assemble the accessories side rails boards and lifting pole F Passing the motor leads inside Assembling the jack and the clip pin see photo above positioning the leads H 15 06 2011 6 28 IAL3L 07 08 11 MEDICATLANTIC 3 3 LIST
11. d not be knotted Only use original parts and accessories supplied by MEDICATLANTIC to guarantee safety and maintain product conformity The bed must not be modified Abnormal use of the bed may damage it or cause accidents to users in which case the warranty shall be annulled Abnormal use means failure to comply with the precautions for use maintenance instructions and other uses not related to the bed s normal purpose such as use of the bed by several people at the same time use outdoors moving the bed on a slope that is steeper than 10 etc 15 06 2011 17 28 IAL3L 07 08 11 MEDICATLANTIC Manufacturer s declaration and guide electromagnetic emissions The medical bed see references in contents has been designed for use in the electromagnetic environment specified below The user should ensure that it is used in such an environment RF emissions The medical bed see references in contents uses RF energy only for its internal functions CISPR 11 Therefore its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment RF emissions Class B The medical bed see references in contents can be used in all domestic environments including CISPR 11 those directly connected to the public low voltage power supply network that supplies buildings for domestic purpose Harmonic emissions Class A EN 61000 3 2 Voltage fluctuations Flicker Applicable EN 61000 3 3 RF emissions
12. ed to ensure proper application of this warranty and also to avoid any invoicing 5 5 IDENTIFICATION Product identification MEDICATLANTIC 4 Manufacturer DOMUS Ai SE lt _ CE marking Serial number and di 4 Refer to user s manual date of manufacture H Address Safe operational load Refer to user s manual TIENS 5 6 LIFETIME gt The beds lifetime under normal conditions of use and maintenance is 5 years 15 06 2011 25 28 IAL3L 07 08 11 MEDICATLANTIC CONDITIONS FOR SCRAPPING gt The product must be scrapped if the main requirements are no longer met particularly when the product no longer has its original characteristics and has not been subject to corrective action during the manufacturing process gt Measures should therefore be taken to ensure that the bed is no longer used for the purpose it was originally intended gt When scrapping the current environmental standards must be complied with 15 06 2011 26 28 IAL3L 07 08 11 MEDICATLANTIC 15 06 2011 2 7 28 IAL3L 07 08 11 MEDICATLANTIC 15 06 2011 28 28
13. eferences in contents wants to be able to 70 Ur for 500 ms 70 Ur for 500 ms continue to use the bed during interruptions in the main power supply it is lt 5 Ur for5s lt 5 Ur for5s recommended that the bed be powered by a converter or battery Power frequency 3 A m 3 A m Power frequency magnetic fields should be at levels characteristic of a typical magnetic field 50 60 Hz location in a typical commercial or hospital environment NB U is the nominal value of power voltage applied during the test Manufacturer s declaration and guide electromagnetic immunity The medical bed see references in contents has been designed for use in the electromagnetic environment specified below The user should ensure that it is used in such an environment CEI 60601 Compliance level Electromagnetic environment Guide Immunity test Severity level Portable and mobile RF communications equipment should be used no closer to the medical bed see references in contents including leads than the recommended separation distance calculated using equations applicable to the frequency of the transmitter Recommended separation distance Conducted RF 3 Vrms 3V LI74P EN 61000 4 6 150 kHz to 80 MHz d 7 Radiated RF 3 V m 3 V m d 1 174 P 80MHzto 800 MHz EN 61000 4 3 80 MHz to 2 5 GHz 90 10 00 Ming i d 2 334 P 800 MHz to 2 5 GHz eee one where P is the maximum output power rating of the transmitter in watts W according to the
14. g pole in good condition positioning and strap Mechanical leads in good condition y Sleeping surface in good condition bed base Y Boards lock and tighten well head and footboards Chest rest functions properly Leg rest functions properly Manual leg rest functions properly TR RTR positions function properly Bed base extension functions properly Castors function properly pivoting rolling etc including the steering castor where applicable Bed immobilises properly castor brakes etc DEBE Verification of tightenings diverse nuts and bolts pins pivot IV stand LL Qualitative aspects YES NO 1 Verification that welds are in good condition 15 06 2011 21 28 IAL3L 07 08 11 MEDICATLANTIC Absence of sound disturbances squeaking lubrications Pf Electrics hydraulics and pneumatics l1 l1 2 Electrical leads plugs and connectors are in good condition not sheared not caught etc Electrical parts in good condition leads motors boxes etc ll Hydraulic and pneumatic parts in good condition pumps compressors jacks dampers etc Remote controls displays and lights in good condition O io Bed specific side rails 1 The rails in place and specific to the bed and or comply with the manufacturer s specifications Properly positioned and secured DS Side rail locking functions properly in raised position CT 1T Check that the height me
15. getting caught between the moving parts of the bed See photo below Clip to secure the power lead 15 06 2011 3 28 IAL3L 07 08 11 MEDICATLANTIC 3 2 DISMANTLING ASSEMBLING THE ALDRYS EVOLUTION BED for divisible bed base gt Separate braking of wheels The brake on the 4 castors must be locked when the bed does not need to be moved Check that the wheels are locked by trying to move the bed If this is not done the patient or another person who leans on the bed may fall A A Braking press down on the brake with your foot J B Releasing the brake press down on the release lever with your foot Centralised braking of wheels The centralised braking of the bed must be activated when the bed does not need to be moved A Braking Push the pedal to the right of the bed with your foot Before transporting or dismantling the bed make sure the back and leg rests are fixed to the frame of the bed base 15 06 2011 4 28 IAL3L 07 08 11 MEDICATLANTIC gt Dismantling the Aldrys Evolution bed for divisible bed base 1 Brake the castors and lift the bed to its highest position Dismantle the accessories lifting pole side rails and boards 3 Unplug the electric lead of the leg rest motor Use a screwdriver to release the jack wire A 4 Remove the clip in the middle of the two 72 bed bases Loosen the Rondo screws and pull the foot half of the bed base towards the feet en
16. he end of the tibia section stays in contact with the bed base 4 6 PRECAUTIONS FOR USE Before use it is essential to read these instructions carefully They contain advice on using and looking after the bed to guarantee optimum safety The user and staff must be aware of the risks associated with using the bed and children must not be allowed on it Although the bed is EMC conforming some devices may alter how it functions in which case they must be used at a distance or not used at all The bed is a medical device and must not be modified under any circumstances You must ensure its traceability including that of the boards and its accessories If you assemble different types of medical devices you must conduct a risk analysis and make the CE declaration 15 06 2011 16 28 IAL3L 07 08 11 MEDICATLANTIC The electric parts jack supply box wired handset etc shall only be repaired by the manufacturer Linak The bed is not suitable for use with an inflammable anaesthetic mixture with air or oxygen or nitrous oxide After each use and while care is being administered to the patient the 4 brakes must be activated to secure the bed When the patient is resting the bed must be placed in its lowest possible position to reduce the severity of a possible fall and the handset must be locked using the key supplied For greater safety the side rails can be adapted see accessories The loads permitted see bed characterist
17. ics must be distributed evenly over the bed base and include the weight of the boards mattress and different accessories Do not activate all the motors at the same time when the patient is in the bed only one motor is authorised at one time After each time the bed is used it must be placed in low position to protect the patient from injury if the patient s health requires this confused demented or physically weak Do not forget to lock the wired handset The bed should not be used as a stretcher Do not sit on the side of the back rest or leg rest if it s not flat When the bed is placed in low position make sure that there are no objects and no parts of the patient s or carer s body caught between the boards and the ground between the boards and base or between the cross braces When the bed is being moved keep the power lead well away from the ground It must not pass between the cross braces or the base and the bed base With no equipotentiality socket optional the patient must not be connected intravascularly or intracardially with electro medical devices Powering up Connection to the supply box must be done using a mains complying with the standards in force and corresponding to a voltage of use of 230 V The wired handset must be hooked to the headboard when not in use During handling the spiral lead and or power lead should be kept away from moving parts such as the cross brace or back rest and shoul
18. impregnation solutions of the cloths have a microbial effectiveness Bactericide NF EN 1040 Bactericide in the presence of interfering substances NF EN 1276 pr EN 13713 Bactericide in carrier method NF T 72190 spectrum 4 Active on Mycobacterium tuberculosis BK Active on Candida albicans NF EN 1275 Fungicide in the presence of proteins NF EN 1650 Active on herpes virus and Rota virus Leave to dry and protect the equipment from being contaminated by other non disinfected equipment with a film labelled with the date of disinfection Product for external use Do not swallow keep away from heat sources and avoid contact with eyes 15 06 2011 24128 IAL3L 07 08 11 MEDICATLANTIC 5 4 WARRANTIES gt All of our products carry a warranty against any manufacturing defect provided the normal conditions for use and maintenance are complied with gt Labour costs due to changes in structures or parts under warranty are not taken into account gt Please refer to the standard terms of sale for the specific terms of warranty for each product gt Every time you contact us for possible maintenance you must quote us the information on the bed identification label and on the electric parts if these are concerned gt Original parts shall be supplied for replacement within the term of warranty by our customer sales network determining the beginning of the term of warranty gt Defective parts must be return
19. ion distances between portable and mobile RF communications equipment and the medical bed see references in contents The medical bed see references in contents is intended for use in the electromagnetic environment in which radiated RF disturbances are controlled The customer or the user of the bed can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the bed as recommended below according to the maximum output power of the communications equipment ET 1 distance according to frequency of transmitter m Rated maximum power of transmitter 1S0KHzto 80MHz kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz W mi iin E e T oe p ee m 3 70 3 66 3 70 3 66 7 37 7 36 11 70 11 6 11 70 11 6 23 30 23 3 For transmitters rated at a maximum output power not listed above the recommended separation distance d in meters m can be estimated using the equation applicable to the frequency of the transmitter where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer Note 1 At 80 MHz and 800 MHz the separation distance for the higher frequency range applies Note 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people MAINTENANCE CONDITIONS The quality of the medic
20. k that its characteristics are suitable for the bed The cleaning instructions recommended must be complied with The mains plug must be disconnected before the bed is moved When the bed is being moved the lead must not trail on the ground or get caught in the castors Do not pull on the mains leads to disconnect the mains plug During any handling try not to catch the leads of the motors and remote control and do not get them knotted The condition of the leads must be checked frequently If the slightest modification is observed the person in charge for maintaining the bed must be contacted to carry out the necessary repairs If repairs are required the person in charge of maintenance must be contacted Moreover the telephone number of the company to be contacted for any repairs is given in this document 4 1 PURPOSE OF BED Aldrys Evolution beds are not designed for children under 12 or for any other purpose apart from those stipulated below Depending on their configuration Aldrys Evolution beds are intended for home use HAD MAD EPHAD and HPA Aldrys Evolution beds with the emergency flattening option of the back rest and locking of functions are designed for medical care centres 15 06 2011 12 28 IAL3L 07 08 11 MEDICATLANTIC 4 2 GENERAL DESCRIPTION This bed has a headboard and footboard See the types of board on offer in the price list Back rest handle Slatted back rest
21. n of the external appearance traces of damp and good overall condition of protective covers in particular and that the motors and jacks function properly Verification that the bed is in good working order test all functions Verification that the frame bed base and mechanical joints are all in good condition When maintenance is carried out at the patient s home as part of a long term contract the installer must also Check the bed is properly installed check to see that there hasn t been any modification contrary to the safety instructions made by the user since the bed s installation Remind the users of the safety instructions All installation and preventive maintenance operations must be recorded See table model below This record must be kept in a designated area throughout the bed s lifetime 15 06 2011 20 28 IAL3L 07 08 11 MEDICATLANTIC QUALITY INSPECTION OF MEDICAL BEDS a ES ES Type model Identification serial no Mass continuity tester EE Dielectrimeter SS Fault current to patient 1 Qualitative aspects YES NO 1 VISUAL CHECKS General condition Users manual available Good overall condition head and footboards bed corners protective stops General cleanliness General cleanliness O Acceptable state of corrosion given the requirements ofthe user Identificationlabel serigraphy in good condition Mechanical condition 4 Liftin
22. oOo MN M DICATLANTIC Le Pas du Ch teau 85670 SAINT PAUL MONT PENIT FRANCE TEL 02 51 98 55 64 FAX 02 51 98 59 07 EMAIL info medicatlantic fr Website http www medicatlantic fr USER S MANUAL ALDRYS EVOLUTION II BED CONTENTS IAL3L 07 08 11 TRANSPORT CONDITIONS STORAGE CONDITIONS ASSEMBLY CONDITIONS CONDITIONS FOR USE MAINTENANCE CONDITIONS CONDITIONS FOR SCRAPPING 15 06 2011 580034 IAL3L 07 08 11 MEDICATLANTIC TRANSPORT CONDITIONS WARNING When handling the bed base the back and leg rests must be strapped to the bed frame During transportation the bed must be in low position braked strapped and protected by cardboard packing The wired handset and supply lead should be attached to the bed base cross member The head and footboards are protected by cardboard and strapped to the sleeping surface The bed should be transported upright when in its original packaging in compliance with the instructions printed on the packaging Top Bottom Fragile or flat in certain circumstances low height In this case the package must not be stacked gt Packaging dimensions L 2030 W 930 H 510 It is strictly forbidden to stack packages weighing over 60kg m whatever position they are in Before transporting or dismantling the bed make sure the back and leg rests are fixed to the frame of the bed base STORAGE CONDITIONS The bed along with the boards and accesso
23. ponsible for correct application must be informed Failure to comply is not a criterion for a non operational status 3 The manager decides on the actions to take and which people to contact depending on the results of the quality inspection and the comments made 15 06 2011 23 28 IAL3L 07 08 11 MEDICATLANTIC 5 2 CLEANING AND DISINFECTION Pressure cleaning is forbidden Unplug the mains lead Check that all the electrical parts are connected together All the sockets of the supply box must be used otherwise the watertightness of it is not guaranteed Clean the electric covers of the jacks and wired handset straightaway if any bodily fluids particularly urine have sprayed on to them Isolate the medical bed in a disinfection room equipped with a particle filtering system and drain for washing floors and walls after disinfection How to use the WIP ANIOS cloth Carefully wipe the surface to be treated and use a second cloth if the surface is very dirty The surface only needs rinsing in the event of gt subsequent contact with mucous membranes gt possible contact with unwrapped foodstuffs Qualitative compositions The impregnation solution of the WIP ANIOS cloths contains Didecyldimethylammonium chloride lsopropanol 8 p p Fatty alcohol ethoxylate type detergent Physicochemical properties Impregnation solutions of cloths oml per cloth Size 200 mm x 200 mm Microbiological properties The
24. ries must be stored at a room temperature of between 10 C and 50 C and relative humidity of between 30 and 75 Atmospheric pressure between 700hPa and 1060hPa under the same conditions as for transporting ASSEMBLY CONDITIONS INSTALLATION RECOMMENDATIONS This equipment should be installed in accordance with the following recommendations Check that the equipment functions properly test all of its functions after it has been installed Users must be trained in how to use the equipment Users the patient and carers must be aware of the safety instructions to be followed see user s manual 15 06 2011 2 28 IAL3L 07 08 11 MEDICATLANTIC 3 1 SETUP FOR USE Remove the packaging protective devices adhesive tape and packing straps Fit the head and footboards with weights into the ends of the bed base and fix them using the Rondo screws in the corners of the bed base Hook the wired handset onto the headboard by passing the cord over the cross braces as in the photo below to stop them getting caught Put the bed in the designated room foreseeing an appropriate perimeter of use for the different functions variable height especially if the bed has a lifting pole or side rails Brake the castors and plug in the power lead checking that the mains comply with the standards in force and that it is suitable for the supply box voltage Also ensure that the power lead is positioned correctly to prevent any risks of
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