QA4 (POWERED) OPERATORS MANUAL
Contents
1. this document is not to be reproduced in whole or in part without the permission of the copyright owners The company reserves the right to modify or improve the equipment referred to QA4 Powered Operators Manual 4 Battery Charging and Battery Maintenance 16 4 1 Power Cord 3 16 4 2 Charging s 16 4 3 Low Battery Alarm i 17 4 4 Manufacturers Recommendation i 17 4 5 Battery Deep Discharge 17 5 Patient Weight Limits 17 6 K8 Pressure Care Mattress i 17 6 1 Infection Control i 18 7 Cleaning and Disinfecting the Stretcher i s 18 7 1 Cleaning 3 i s 18 7 2 Disinfecting 18 8 Product Maintenance 18 9 Identifying Product Labels and Symbols 3 19 9 1 Common Symbols 3 i 19 9 2 Steer Label R i s i 19 9 3 Brake Label 19 9 4 Leg Section Label s 19 9 5 Head Section Label s s 19 9 6 Articulating Leg Section Label s i 19 Portsmouth Surgical Equipment Ltd and Anetic Aid Ltd All rights reserved this document is not to be reproduced in whole or in part without the permission of the copyright owners The company reserves the right to modify or improve the equipment referred to QA4 Powered Operators Manual 1 1 1 1 2 1 3 Introduction These instructions are intended to assist you with the operation2. 23 05 11 Page 9 QA4 Powered Operators Manual 3 2 5 Using the Leg Section The stretcher comes standard with a non articulating lightweight leg section Fig 2 no 6 if the stretcher has an articulating leg section installed refer to section 3 2 5 3 3 2 5 1 Removing the Leg Section Depress both buttons as shown one button is located on each side of the stretcher and remove the leg section WARNING Ensure that any persons responsible for removing the leg section adopt good posture and stance in accordance with the relevant Moving and Handling policies to prevent injury to the user Push Pull a S A A Fig 8 3 2 5 2 Replacing the Leg Section Engage the locating spigots of the leg section as shown and push firmly until the leg section is fully engaged A WARNING Ensure that the leg section is fully engaged and securely locked in position Fig 9 Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page 10 QA4 Powered Operators Manual 3 2 5 3 Articulating Leg Section To articulate the leg section pull up on the leg frame lever and push down on the board To remove the leg section refer to section 3 2 5 1 NOTE The articulating leg section is an optional accessory for this stretcher CAUTION With the leg section articulated down caution must be exercised when tilting the stretcher leg down i e a reverse trendelenburg position NOTE
3. Manual 9 Identifying Product Labels and Symbols 9 1 Common Symbols The following symbols are used on labels affixed to the stretcher read the following text for an explanation as to their specific meanings This symbol is an instruction to the reader its literal meaning is Consult Operators Manual wherein the operating instructions provided with the stretcher will provide further information and clarification This symbol is an instruction to the reader but carries more force than the previous symbol its literal meaning is Attention Consult Accompanying Documents wherein the operating instructions provided with the stretcher will provide further information and clarification This symbol indicates the safe working load of the stretcher and the removable components i e the leg and head sections 9 2 Steer Label The steer label indicates the position of the fifth wheel steering mechanism and that depressing the pedal downwards engages the steering mechanism 9 3 Brake Label The brake label indicates the position of the brake mechanism and that depressing the brake pedal downwards engages the brakes 9 4 Leg Section Label The leg section label indicates that the lightweight leg section can be removed 9 5 Head Section Label The head section label indicates that the angle of the removable head section can be adjusted 9 6 Articulating Leg Section Label The articulating leg section label indicates th
4. With the articulating leg section the leg section should be articulated down to the maximum angle before being removed This shortens the distance between the end of the leg section and the mounting sockets This does two things one it provides better access to the release buttons and two it reduces the distance that the user has to reach to support the weight of the articulating leg section NOTE When replacing the articulating leg section pull the actuation handle to operate the gas struts and allow the location spigots to achieve a horizontal position 3 2 6 Using the Stretcher Sides The stretcher comes standard with four stretcher sides Fig 2 no 7 that can be individually removed from the stretcher or rotated through 180 degrees Each side is mounted into a fixed socket that is labelled with a position number 1 4 this corresponds with the numbered label on the stretcher side and ensures that each stretcher side is correctly positioned See the following sections for more information on rotating removing and replacing the stretcher sides 3 2 6 1 Rotating the Stretcher Sides Depress the button as indicated see Fig 10 and rotate the stretcher side the side will automatically relock in the next position Rotate Push Fig 10 Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page 11 QA4 Powered Operators Manual 3 2 6 2 Removing the Stretcher Sides Ensure the stretche
5. has been classified as a Class 1 device Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page 1 QA4 Powered Operators Manual 2 Product Specifications F C SERIAL NUMBER LABEL mode 3 G a H Fig 1 Key to Fig 1 Weight Limits A Height MIN 23 75 Stretcher 550 Ibs Height MAX 39 5 Head Section 55 bs B Mattress Length 80 25 Leg Section 110 Ibs C Stretcher Length 82 75 Stretcher Weight 350 Ibs D Mattress Width 23 5 Castor Diameter 6 E Stretcher Width With Side Rails 25 75 Fixed Leg Section Standard F Stretcher Width With Sides 30 25 Weight 13 25 G Stretcher Width Brakes Off 32 75 Articulation N A H Base Length 46 75 Articulating Leg Section Optional Mattress Depth 3 Weight 17 5 lbs Trendelenburg 20 Articulation 0 45 Reverse Trendelenburg 12 Lateral Tilt 12 12 Backrest Articulation 0 65 Head Section Articulation 30 30 Head End Top Slide 9 Foot End Top Slide 9 O Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page 2 QA4 Powered Operators Manual 3 Product Functions Fig 2 Key to Fig 2 1 Hand control 2 Brake Pedals 3 Steering Pedal 4 Lateral Tilt Handle 5 Head Section Tilt Actuation Lever 6 Removable Leg Section 7 St
6. there are no obstructions in the way before traversing the patient platform A CAUTION With the leg section folded down caution must be exercised traversing the patient platform towards the head end CAUTION When the head section is in the folded away position caution must be A exercised when traversing the patient platform There is a possibility that the head section could clash with other parts of the stretcher which may result in permanent damage being caused to the stretcher AREAS OF C ARM ACCESS iN d o i E N N 4 Sw CENTRAL i OO LIMN 7 AREA Ww Uy pH La i m SS SS CENTRAL EI SS COLLMN d a N AREA N s Lu Q A NN Ww e i WSN TARER FOOT END TRAVERSED TZ Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page 6 QA4 Powered Operators Manual 3 1 5 Using the Trendelenburg Function The patient platform can be longitudinally tilted to provide a trendelenburg head down or reverse trendelenburg leg down position by using one of the two down buttons on the hand control The head down trendelenburg button is in filled in red to indicate that this button is used for emergency positioning A CAUTION Ensure that there are no obstructions in the way before tilting the patient platform CAUTION Ensure that there is no equipment stored in the base moulding of the stretcher before tilting the pat
7. 2 NOTE the manufacturer recommends that a spare hand control is purchased and stored in an accessible location in the event that the hand control becomes damaged CAUTION Because the hand control is in constant use it is particularly vulnerable to wear A and tear or damage Before use it is important to inspect the hand control to ensure there is no damage to the cable or the buttons A WARNING In the event of hand control damage the hand control should be replaced immediately or the stretcher removed from service WARNING Hand control damage may lead to malfunction during equipment use If a hand control button becomes damaged it is possible for one of the powered functions to operate spontaneously In this unlikely event the following actions should be taken A 1 Depress and hold the opposing function button i e if the backrest is raising press backrest down 2 Unplug the hand control from the stretcher 3 Attach anew hand control 4 lf another hand control is not available transfer the patient to another stretcher 3 1 2 Height Adjustment The height of the patient platform can be adjusted by using the up and down buttons on the hand control When either button is depressed the green indicator light on the hand control will illuminate to indicate that the stretcher is powered A CAUTION Ensure that there are no obstructions in the way before raising or lowering the patient platform A CAUT
8. ION Ensure that there is no equipment stored in the base of the stretcher before lowering the patient platform 3 1 3 Using the Backrest The backrest can be raised and lowered by using the up and down buttons on the hand control CAUTION Ensure that there are no obstructions in the way before raising or lowering the backrest Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page 5 QA4 Powered Operators Manual 3 1 4 Patient Platform Top Slide C Arm Access Fig 4 The patient platform is designed to slide longitudinally either towards the head end or the leg end to provide full C arm access a gynaecological position and improved access at the head end The patient platform is traversed by using the left and right buttons on the hand control The mattress and patient platform are made from X Ray translucent materials The areas of C arm access are illustrated in Fig 4 with the stretcher traversed in both directions The stretcher should be returned to the neutral position once the procedure has been completed Observe that when the patient platform is traversed in either direction the mid section static frame arm is revealed In the neutral position the traversing section of the patient platform aligns with the static arm NOTE The patient platform should be returned to the neutral position once the procedure has been completed see above A CAUTION Ensure that
9. QA4 POWERED OPERATORS MANUAL Me DITEK A We re here for life QA4 Powered Operators Manual Contents Page 1 Introduction i A 1 1 1 Warnings and Cautions s 1 1 2 Scope of Use 7 1 1 3 Equipment Classification i 1 2 Product Specifications 2 3 Product Functions 3 3 1 Powered Stretcher Functions 4 3 1 1 Using the Hand Control 5 3 1 2 Height Adjustment 5 3 1 3 Using the Backrest 5 3 1 4 Patient Platform Top Slide C Arm Access 6 3 1 5 Using the Trendelenburg Function 7 3 2 Manual Stretcher Functions 8 3 2 1 Using the Brakes 8 3 2 2 Using the Steering Pedal 8 3 2 3 Using Lateral Tilt 8 3 2 4 Using the Head Section 9 3 2 5 Using the Leg Section 10 3 2 5 1 Removing the Leg Section 10 3 2 5 2 Replacing the Leg Section 10 3 2 5 3 Articulating Leg Section optional 11 3 2 6 Using the Stretcher Sides A 11 3 2 6 1 Rotating the Stretcher Sides 11 3 2 6 2 Removing the Stretcher Sides 12 3 2 6 3 Replacing the Stretcher Sides 12 3 2 6 4 Attaching the Full Length Stretcher Side 13 3 2 6 5 Rotating the Full Length Stretcher Side 13 3 2 7 Using the Emergency Backrest Release Function 14 3 2 7 1 Releasing the Emergency Backrest Handle s 14 3 2 7 2 Reengaging the Emergency Backrest Handle 15 3 2 8 UsingthelV Pole 15 Portsmouth Surgical Equipment Ltd and Anetic Aid Ltd All rights reserved
10. at the leg section can be articulated and removed NOTE The articulating leg section is an optional accessory for this stretcher BE AN D A v ES O Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page 19 Do not lift by brake pedals or top lift from base frame only Important Battery Information Before Use The stretcher must be charged for 8 hours Storage The stretcher must be charged for 8 hours every 2 weeks Failure to do so will result in permanent battery damage See section 4 Battery Charging amp Battery Maintenance for further instruction Me DIT Ge K S J e We re here for life 1810 Ellice Avenue Winnipeg MB R3H 0B7 T 1 800 567 8400 F 1 204 779 4900 www mediteksurgical com 2 10 18 2012
11. fective pressure care properties of the mattress will decline below satisfactory levels after 4 years at which time we recommend the mattress be replaced NOTE An independent pressure care report produced by Salford University is available upon request O Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page 17 QA4 Powered Operators Manual 6 1 7 7 1 7 2 Infection Control Ultrasonic welding of materials creates an impervious seal ensuring an ideal product for infection control Each mattress part is attached to the patient platform with Velcro this enables the mattress sections to be removed from the stretcher for cleaning and replacement NOTE The mattress parts should be visibly inspected for damage on a daily basis If the outer mattress fabric is torn then fluids will penetrate and the mattress should be replaced Do not attempt to repair tears or splits with self adhesive tapes Cleaning and Disinfecting the Stretcher Cleaning The stretcher should be wiped over thoroughly after each use with warm water and neutral detergent and then wiped dry using a soft cloth adequate drying is crucial in the care and maintenance of this product Disinfecting The stretcher should be wiped over thoroughly with warm water and disinfectant diluted chlorine or alcohol based solutions are suitable for this purpose as is a 1 solution of sodium hyperchloride Always ensure that the disi
12. going to be placed in storage the stretcher must be charged for eight hours every two weeks Failure to do so will result in permanent battery damage A CAUTION Only batteries supplied and approved by Meditek should be used A CAUTION The battery unit should not be opened A CAUTION Use the battery only for its intended purpose A CAUTION Never use a battery that is damaged A CAUTION The battery must be recycled properly disposed of or returned to Meditek The battery must not be discarded with general waste Power Cord The stretcher is supplied with an IEC power cord which is used to charge the on board battery A WARNING Only use the power cord supplied with the stretcher for charging purposes Do not use the power cord for any other purposes A WARNING Visually inspect the power cord for damage on a daily basis Do not use the power cord if damaged in any way Charging The power cord should be plugged into an electrical socket and the appliance connector end plugged into the charging socket on the stretcher Fig 2 no 11 The socket should now be switched on Once the power cord is connected the control unit will check the charge capacity of the battery before commencing charging this may take up to 12 minutes Once this test is complete the battery will either begin to charge and the battery status LED on the hand control will flash green or the battery status LED wil
13. hand control WARNING Ensure that the handle is properly reengaged Failure to do so will result in the backrest not functioning correctly and possibly disengaging unexpectedly Using the I V Pole The stretcher comes standard with a loose I V pole that can be attached at any point along the side bar and secured using the hand wheel To adjust the height of the I V pole as illustrated in Fig 16 grasp the locking mechanism A and using your thumb lift the mechanism to release the lock and move the pole up or down to the required height B release the mechanism to lock the pole in position CAUTION When adjusting the height of the pole use two hands one to adjust the height of the inner pole and hooks and the other to hold the outer pole to ensure that it remains fully engaged in the mounting socket The I V pole is fitted with two spring loaded hooks that are designed to return to their original upright position when not in use Swivel one or both hooks outwards C to hang the I V bags O Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page 15 QA4 Powered Operators Manual 4 4 1 4 2 Battery Charging and Battery Maintenance As with all products that use a rechargeable battery the battery will require recharging at regular intervals The frequency with which the battery requires recharging is dependant on the battery usage and the state of charge If the stretcher is
14. ient platform NOTE This ONLY applies when the stretcher is at its lowest height Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page7 QA4 Powered Operators Manual 3 2 Manual Stretcher Functions The following functions are manually operated and are not powered from the on board battery supply or main power supply 3 2 1 Using the Brakes All four castors are locked simultaneously by depressing either of the brake pedals Fig 2 no 2 at any point along the length of the pedal The brakes are disengaged by lifting either pedal 3 2 2 Using the Steering Pedal The stretcher can be manoeuvred more easily by engaging the steering mechanism The mechanism is engaged by pressing the steering pedal Fig 2 no 3 and disengaged by lifting the pedal A CAUTION Applying the steering pedal with excessive force i e by standing on the pedal will cause permanent damage to the mechanism CAUTION The steering pedal is designed to disengage automatically when the stretcher A is pushed leg first over an obstruction Attempting to prevent this will cause damage to the mechanism The 5 wheel should be allowed to disengage and then can be reengaged after the obstruction A CAUTION The steering wheel must be disengaged manually when the stretcher is pushed head first over an obstruction i e an elevator threshold or damage may occur 3 2 3 Using Lateral Tilt Lateral tilt is achieved by
15. l turn solid green to indicate that the battery is fully charged From empty the battery will take approximately 8 hours to fully charge Plugging the stretcher in for a short period of time will only partially recharge the battery The stretcher can be left on charge permanently as there is no danger that the battery can be over charged The control unit manages the status of the battery charge switching the charging circuit off when the battery is full and back on when the charge dissipates below a pre set level Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page 16 QA4 Powered Operators Manual 4 3 4 4 4 5 Low Battery Alarm When the battery charge is low the control unit will emit a continuous beeping tone when any one of the function buttons is being depressed and the hand control battery status LED will turn amber This indicates that the battery must be recharged failure to do so will result in the deep discharge protection being enabled CAUTION Failure to charge the battery once the low battery alarm has sounded could result in a permanent loss of maximum charge capacity Manufacturers Recommendation We recommend that the battery is put on charge whenever the stretcher is not in use including overnight Establishing this routine will ensure that the stretcher does not run out of charge in the course of a day Battery Deep Discharge If the battery has not bee
16. n charged and the stretcher is continuously used the battery will run flat and eventually reach a deep discharge condition A normal 8 hour charging period will not be sufficient to recover the battery The battery will need to be on charge for approximately 72 hours to fully recover Patient Weight Limits 1 Main Body The stretcher is designed to accommodate a maximum patient weight of 550 Ibs Patients should mount the stretcher at the centre of the patient platform and their weight kept as evenly distributed as possible whilst on the stretcher 2 Head Section The head section is designed to take a maximum weight of 55 Ibs 3 Leg Section The leg section is designed to take a maximum weight of 110 Ibs WARNING Exceeding any of the maximum specified weight limits could result in failure of the stretcher and injury to the patient and staff K8 Pressure Care Mattress Understanding the needs for greatest possible patient pressure area care the mattress is manufactured using the most up to date materials and manufacturing methods available They consist of 1 Body Mould Visco Foam Through its sensitivity to temperature this gel feel foam actually moulds to the patient s body relieving pressure by distributing the load as evenly as possible 2 Flexi Fabric A polyurethane water resistant vapour permeable outer cover with the properties of Lycra ensures maximum effect of the body mould foams 3 Pressure Care Properties The ef
17. nfectant manufacturer s guidelines are followed Following disinfection wipe the stretcher thoroughly with warm water and dry with a soft cloth This is very important as adequate drying is crucial in the maintenance of this product CAUTION Do not use strong bleaching disinfectant solutions organic solvents abrasive powders or expose materials to excessive heat Product Maintenance It is recommended that the stretcher is serviced on an annual basis in accordance with the manufacturer s service schedule For details of extended warranties and service programmes please contact Meditek Before use ensure all stretcher functions operate to their full range of movement and that all detachable components disengage re engage and lock correctly Because the hand control is in constant use it is particularly vulnerable to wear and tear or damage Before use it is important to inspect the hand control to ensure there is no damage to the cable or the buttons see section 3 1 1 Using the Hand control for more information NOTE The manufacturer recommends that a spare hand control is purchased and stored in an accessible location in the event that the hand control becomes damaged Also visually inspect the stretcher for any loose or damaged parts foreign objects caught in the castors and hydraulic fluid leakage Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page 18 QA4 Powered Operators
18. of the QA4 Day Surgery Stretcher It is important that these instructions are read thoroughly before using the equipment It is also important to check the stretcher before use ensure that all stretcher functions operate to their full range of movement and that all detachable components disengage re engage and lock correctly We recommend that the stretcher is visually inspected for any loose or damaged parts foreign objects caught in the castors and hydraulic fluid leakage Warnings and Cautions Various warnings and cautions are made throughout these operating instructions A WARNING is given when the personal safety of the patient or user may be affected and when disregarding this information could result in injury A CAUTION is given when special instructions must be followed Disregarding this information could result in permanent damage being caused to the stretcher Scope of Use This product is intended for use within a day surgery environment for the induction transport treatment and recovery of patients Due to its extra functionality and higher weight capacity this stretcher is heavier than a conventional patient transfer stretcher and therefore less suitable for this function In addition the stretcher has very low ground clearance that may cause problems when traversing uneven ground A CAUTION The stretcher may be damaged by pushing it across rough or uneven ground Equipment Classification The stretcher
19. retcher Sides 8 Pushing Handles 9 Oxygen Cylinder Mounting Trough 10 V Mounting for Suction Canister 11 Power Input Charging Socket 12 Hand control Socket 13 LV Pole Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page 3 QA4 Powered Operators Manual 3 1 Powered Stretcher Functions The following four stretcher functions are electromechanical in operation and are powered from an on board battery supply These functions are operated and controlled through the hand control Fig 2 no 1 the layout of the hand control is shown below CAUTION The battery must be properly maintained in accordance with these A instructions Failure to do so will result in significant loss of charge capacity or failure of the battery Refer to section 4 Battery Charging and Battery Maintenance for a full explanation on how to care for the battery Fig 3 Key to Fig 3 Battery Status LED Variable Height Functions Backrest Articulation Functions Patient Platform Top Slide Functions Trendelenburg amp Reverse Trendelenburg Tilt Functions Logo oO miitwNA O Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page4 QA4 Powered Operators Manual 3 1 1 Using the Hand Control The hand control is externally removable and plugs into the hand control socket on the base of the stretcher at the head end Fig 2 no 1
20. rotating the lateral tilt handle Fig 2 no 4 either clockwise or counter clockwise To use the lateral tilt handle extend the handle by pulling it away from the stretcher and unfold the crank handle until it locks into position Return the handle to its stored position when not in use CAUTION The lateral tilt handle must be stored away to ensure that the handle does not get damaged Rotate Fig 5 Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page 8 QA4 Powered Operators Manual 3 2 4 Using the Head Section The head section is articulated by simply pulling up on the head section tilt actuation lever The head section is also designed to be removed for specific procedures i e gynaecology and urology to give greater anaesthetist access to the patient Removing the head section prior to administering anaesthetic reduces the length of the backrest and the need to reposition the patient in surgery Removing the head section also gives greater access to the patient from the head end for staff Lower Fig 6 Remove Fig 7 The head section is removed by lifting the release handle then lowering and removing the head section from the support bracket WARNING When the head section is attached to the stretcher ensure that the head section is fully engaged and securely locked in position Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26
21. rs Manual 3 2 7 Using the Emergency Backrest Release Function The emergency backrest release handle allows the backrest to be dropped immediately from any articulated angle to the horizontal position When the emergency backrest release handle is disengaged the backrest will not function the backrest handle must be engaged for correct backrest operation NOTE It is important that staff are clearly informed as to the location of the emergency release handle its function and its mode of operation 3 2 7 1 Releasing the Emergency Backrest Handle Grasp the emergency release handle and rotate the handle counter clockwise As the handle is released the backrest will be unsupported and will drop to the horizontal position WARNING Caution is required when releasing the emergency backrest handle Once the handle is released the backrest will fall without resistance ensure no persons are stood behind or under the backrest when the handle is released LN Fig 15 Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page 14 QA4 Powered Operators Manual 3 2 7 2 Reengaging the Emergency Backrest Handle 3 2 8 Fig 16 Manually lift the backrest until it stops Grasp the emergency release handle and rotate the handle 90 degrees clockwise until the handle clicks into position and physically stops The release handle is now reengaged enabling the backrest to be operated from the
22. rs side is in the up position depress the button as indicated see Fig 11 and remove the stretcher side Lift Push Fig 11 3 2 6 3 Replacing the Stretcher Sides Align the stem of the stretcher side to the socket and let the stretcher side drop into position the stretcher side will automatically lock in position when replaced CAUTION Ensure that the stretchers sides are located into their respective numbered sockets to prevent the stretcher sides clashing Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page 12 QA4 Powered Operators Manual 3 2 6 4 Attaching the Full Length Stretcher Side The optional full length stretcher side attaches to the stretcher by hooking onto the side bar To secure the stretcher side rotate the locking clamp handle 90 in either direction shown in Fig 13 WARNING Failure to secure the stretcher side to the side bar using the locking clamp could result in injury to the patient I Fig 12 Fig 13 3 2 6 5 Rotating the Full Length Stretcher Side When the stretcher side is secured to the stretcher as shown in Fig 13 pull the handle in the up direction as indicated in Fig 14 and rotate the stretcher side away from the stretcher into the down position The stretcher side will automatically relock in the down position Fig 14 O Portsmouth Surgical Equipment Ltd Document No 992010 Issue 26 23 05 11 Page 13 QA4 Powered Operato
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