300 Series Procedure Chair Manual
Contents
1. Please follow local regulations and laws when disposing of the electrical components used in this chair For all Customer Service related problems refer to the Service Manual WARRANTY View complete warranty details at www oakworks com 12 MODEL NUMBER amp SERIAL NUMBER MODEL amp SERIAL NUMBERS The model number and serial number are located on the seat acrylic on the backside of the chair Procedure Tables and Chairs Model Number a ULM UOI LILI J Intertek 3034177 1 n CONFORMS TO i 16796025 PC30G32719743MTTZZH8BK i ae A Serial Number Ser PC1565022 Certified 10 CANICSA STD PCM 300 Series 27 x 19 35 x 74 3M TT XXH8BK 1 TTSKYBLUE 01 04 2013 Order 654321 Notes Sample Product Label European Authorized Representative mergo Europe The Hague 2513 BH Power Rating US 120 V 60 Hz Netherlands Duty Cycle MAX 2 minutes ON 18 minutes OFF A Class 1 Equipment ree 923 East Wellspring Rd Deere OAKWORKS New Freedom PA 17349 USA MEDIC A L Phone 717 235 6807 Part No 70537 7 rev C www oakworks com Model Numters and Serial Numbers always start with a letter MODEL NUMBER DESCRIPTION PC30G3XXXXXX3MITT XXXX Options Spaces not used Fabric Terra Touch Padding A3 3 8 cm Comfort Foam A4 4 10 cm Comfort Foam Table Top Length Minimum Table Height Table Width Top 3 section Back Rest Base 30 Standard Base SW Swivel Base Procedure C2. lbs 68 kg Clamp amp pole not included DIRECTIONS FOR USE ARM REST INSTALLATION AND ADJUSTMENT C AUTI O N Do not use the arm rest for patient support during the mounting or dismounting of the chair The arm rest is not designed to support the patients weight TO INSTALL THE ARM RESTS The Arm Rests adjust automatically as the back rest moves to remain parallel to the floor 1 Insert end of arm rest into back 2 Push end all the way into the hole and drop the arm rest into the horizontal rest hole while holding the arm position Pull outward to make sure the arm rest is secure rest at a 60 angle to the backrest To remove the arm rest simply reverse the procedure above If the Arm Rest s are not level Refer to the Service Manual PAPER ROLL HOLDER USE To load the paper locate the two Insert rod through paper roll and place Pull paper and thread through the paper holder support arms located rod into the holes in the support arms straps across the upholstered top to on the underside of back rest keep in place Note The paper hold down strap is attached with Velcro This allows strap tension adjustment if necessary DIRECTIONS FOR USE PROCEDURE CHAIR FACE REST CRESCENT The Procedure Chair Face Rest Crescent is designed to be used for prone positioning An Adjustable Head Rest is required for this accessory T RAIL ADAPTER The T Rail Adapter can be attached at designated locat
3. 0 0 00 ccc cecccceeccceeccceeececeeecceuecssuceseeceseeeceseeeeeeeeceueeeegs 12 Warranty Information wisisiccssscteasatindssosaiics cincaadds Deadintoradncbaaaoaniocneddubsdconsaddauendeadaaiencieaabareada 12 Model Number amp Serial NUMDET 0 ccc cceccceeecceeeceeeeceseeecseeeseeeeeseeeeeegs 13 Specifications e a IICA OIG T E E A E EE ETET 14 Environmental Conditions ccecceea tees cccteesuestcmestccwwxed aE A E ETE R 14 Pleciricak opec NONIS eenen ri ar E OE E E A A A E EAT 14 Guidance and manufacturer s declaration Electromagnetic emissions serrerrieeeririiei rinnen Eo r EET E NAROA r Eria 15 Recommended separation distanc s c ssscisswndscspososianincasansasendemate nevsndossdiaenslscsesnaeeaeesn 15 Guidance and manufacturer s declaration Electroma menc minniy sanesscsacenoadscseebeancrance n o E e EE 16 17 Revision HISTOTY ccc cccccceeccceeccenecceecceeeceenceeeeceeneceeeccenceceuceeeeceeuceeeecesacesenseeneeeeneeageees 20 CONTACT Information 0 0 cose ccc cc ccc ec eccccccececcccecececcececesccceccacuececsescecesesescecaseeees back cover PRODUCT USE DESCRIPTION IMPORTANT SAFETY INSTRUCTIONS PRODUCT USE DESCRIPTION The Procedure Chair is a powered positioning examination table used to support the patient during medical procedures It is intended to be operated by a healthcare professional in a medical environ ment No special training is required but a review of the following Safety Instruct
4. 5 UT gt 95 dip in UT gt 95 dip in UT for 5 sec for 5 sec Power frequency magnetic fields should be at levels characteristic of a typical location in a typical com mercial or hospital environ ment NOTE Ur is the a c mains voltage prior to application of the test level Power frequency 50 60 Hz magnetic field IEC 61000 4 8 SPECIFICATIONS Guidance and manufacturer s declaration electromagnetic immunity The chair is intended for use in the electromagnetic environment specified below The customer or the user of the chair should assure that it is used in such an environment Immunity Test IEC 60601 test level Compliance level Electromagnetic environment guidance Portable and mobile RF communications equipment should be used no closer to any part of the chair in cluding cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Recommended separation distance d 1 2VP d 1 2V P 80 MHz to 800 MHz d 2 3V P 800 MHz to 2 5 GHz Conducted RF 3 Vrms Where P is the maximum output power rating of the BE er E E MARE transmitter in watts W according to the transmitter Radiated RF 3 V m manufacturer and dis the recommended separa IEC 61000 4 3 80 MHz to 2 5 GHz NS A E A Field strengths from fixed RF transmitters as deter mined by an electromagnetic site survey should be less than the compliance level in each frequency
5. TABLE OF CONTENTS Product Use Description 000 00 ccc cecccceseccceeecceeceeeeceeeecsueeeseeesseeeceseecesaeeceeeeeetens 1 Important Safety Instructions DYNO CTC a a cece princes E A auteutecenee neuen A ET 1 BCE PS Oh Spats sre tect cde ators E E E E 1 2 Product Description amp Photo 300 Series Procedure Chairt ssirecncsscvicecescesdessvesu vee sudereucussvnsideoassancweedeua vabiesdesbcossuendewaaaocs 3 Installation 0 bugis E N eee ce E eer E ee E A 4 Directions for Use Fee GOON i AOS cacti ge ssnee oyaeee acetates ate secre sear ear pe ete etaetnerter eee eeoiers 5 POOE ORE Ol OD Cl AION Sis rac ssczosocaevse sess E E E ioe E E cates 6 Swivel Bose lt n ee Oe ee eee eerie ee ne ee ee 7 Retractable Foot Rest stirrup 1 Se siceiniienicorerina ti 7 Haad Rer U ee EE E ais eeaneasechueeteabeweaces 8 Procedure Tray Uo eera A E E E 2 e S IRL E E E E OE A semen E EA E 9 Anm Rest instalaionr and AC jUSt Ve sosstence seen sccoeswss E ES 10 Peper RORO EE as casera E E E E E E E 10 Procedure Chair Face Rest Crescent cccccccccccceccecescsccuscscescescusescessescescusessesseseusens 11 MATRA ECO VOW aeaates xa tener sarasota tas ae tera E E aero ence E E 11 Power Outlet Use issssononsnesesesesesesesssrsresesesesesesesresesesesesesesossesesesesesesoeoseesesesesesoseseeee 11 Cleaning amp Disinfection 000nnnnoeeeennnnssseeensssssstersssessersssssstressssseeressssssrrsssssssreesssseeeoo 12 Inspections amp Maintenance
6. able Large Head Rest 11 5 long x 20 wide 29cm x 51cm removable T Rail Adapter Attaches to the backrest on one or both sides Procedure Chair Face For prone use adjustable head rest required Rest Crescent Auto level design adjusts to backrest angle swing out 90 24 Lg x 5 W 61 x 13cm removable For electrical specs see Specifications section Arm rests 2 3 INSTALLATION The Procedure Chairs come completely assembled and ready to use Plug the cord into a functioning out let that is rated for the table see Grounding below Arrange the power cord and control cords so that they will not create a tripping hazard and where the controls are located to your liking and are conveniently accessible Be sure access to plug is not blocked for disconnecting the table from power GROUNDING A D ANGE R Risk of Electric Shock Connect this furnishing to a properly grounded outlet only This product must be grounded If it should malfunction or break down grounding provides a path of least resistance for electrical current to reduce the risk of electric shock This product is equipped with a cord having an equipment grounding conductor and a grounding pin The pin must be plugged into an appropriate outlet that is prop erly installed and grounded in accordance with all local codes and ordinances See U S sample below Grounding Methods ss SROurrpep AUTLET pox faa for CHRHDMHG Sone vA Corr
7. blishments other than domestic and those directly con IEC 61000 3 2 nected to the public low voltage power supply Voltage fluctuations network that supplies buildings used for domestic flicker emissions Complies purposes IEC 61000 3 3 Recommended separation distances between portable and mobile RF communications equipment and the chair The chair is intended for use in the electromagnetic environment in which radiated RF disturoances are controlled the customer or the user of the table can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the chair as recommended below according to the maximum output of the communications equipment Rated maximum output power of transmitter 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz 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 maximum output power rating of the transmitter in watts W according to the transmitter manufacturer NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people SPECIFICATIONS Guidance and manufacturer s declaration electromagnetic immunity The chair is intended for use in the electromagn
8. covered under the warranty DO NOT use citrus based cleaners or other strong cleaners such as alcohol acetone higher concentrations of bleach or other products that contain high concentrations of these substances DO NOT expose the fabric to temperatures below 50 F 10 C or above 104 F 40 C DO NOT expose the fabric to direct sunlight adhesives liquids or abrasive materials INSPECTIONS amp MAINTENANCE RECOMMENDED REGULAR INSPECTIONS monthly or local standard e Check for damage to the power hand control or foot control cables e Visually inspect components for obvious damage that could cause problems during operation RECOMMENDED PERIODIC INSPECTIONS yearly or local standard e Check for damage to the power hands control or foot control cables and all visible wiring e Visually inspect components for obvious damage that could cause problems during operation e Check all mechanical functions using the hand control Repeat using the foot control Check for abnormal noises e Replace any missing or illegible labels e Check that all fasteners are present and fastened securely e Check table grounding e Clean unusual buildup of dirt on the chair and or parts of the chair not normally cleaned on a regular basis e Check for tears or cracks in the upholstery MAINTENANCE e No specific maintenance tasks are required e Oakworks medical tables chairs are designed and built to provide many years of dependable service
9. ect Implementation X incorrect Implementation Improper connection of the equipment grounding conductor can result in a risk of elec tric shock Check with a qualified electrician or service person if you are in doubt as to whether the product is properly grounded Do not modify the plug provided with the product if it will not fit the outlet have a proper outlet installed by a qualified elec trician DIRECTIONS FOR USE HAND CONTROL OPERATIONS A C AUTI O Do not sit on the Fowler Backrest or Leg Rest sections Do not leave the patient unat tended When lowering the chair or using the Trendelenburg functions make sure there is nothing that can impede motion like stools cabinets accessory parts cleaners etc The Multi function Hand Control operates all functions by holding down one button at a time Follow the directions below to access these functions If a function button does not release pressing and holding any other function button will stop the motion os A n a Trendelenburg head Reverse Trendelenburg end down up to 15 foot end down up to 5 p Height Up oF Height Down y Back Rest Down Fully down and seated position MEMORY FUNCTION USE Fully up and fai poston M E M Use any of the top 8 buttons to orient the chair in a favorite position Press and release the MEM button twice within five seconds and listen for two quick beeps Your position is now set when
10. esired position up to 240 RETRACTABLE FOOT RESTS STIRRUP USE A C AUTION Pinch Point Keep fingers away from pinch point 1 Fully lower the powered 2 Grasp Stirrup handle amp 3 Fold out to fully open 4 To rotate stirrup to the foot rest to allow access to pull out firmly while lifting position desired angle lift slightly the stirrup slightly Pull fully out and move to the desired position There are 3 detent positions Stop lift ing and move slightly left To store stirrups lift slightly rotate towards the middle of the chair and or right for the nearest fold the foot rest down Then lift slightly and push into the storage position detent position 5 To reduce stirrup length lift the handle slightly and push into desired position Stirrup will automatically lock into nearest detent posi tion DIRECTIONS FOR USE HEAD REST USE A C AUTI ON Do not extend the dowels more than 4 10 cm from the Back Rest section Adjustable Large The Adjustable head rest angle is adjusted using a locking knob The head rest distance from the table is adjusted by using a knob The Large head rest is adjusted by using the knob To adjust the position of the head rest follow these steps Turn knob counter clockwise Move head rest platform to Turn knob clockwise to lock to unlock the cam the desired position the cam HEAD REST ANGLE Adjustable Head Rest only Loosen knob by turnin
11. etic environment specified below The customer or the user of the chair should assure that it is used in such an environment l Electromagnetic Immunity Test IEC 60601 test level Compliance level Floors should be wood a t ic tile ae 6 kV contact 6 kV contact ee a S a synthetic material the rela IEC 61000 4 2 eel ent tive humidity should be at least 30 Mains power quality should be that of a typical com mercial or hospital environ ment Electrical fast transient Sit 2 kV for power supply lines 2 kV for power supply lines IEC 61000 4 4 kV for input output lines Not applicable Mains power quality should be that of a typical com mercial or hospital environ ment surge 1 kV differential mode 1 kV differential mode IEC 61000 4 5 2 kV Common mode 2 kV common mode lt 5 UT lt 5 UT Mains power quality should gt 95 dip in UT gt 95 dip in UT be that of a typical com for 0 5 cycle for 0 5 cycle mercial or hospital environ ment If the user of the chair 40 UT 40 UT requires continued opera Voltage dips short inter 60 dip in UT 60 dip in UT tion during power mains ruptions and voltage for 5 cycles for 5 cycles interruptions it is recom variations on power supply oat 50 UT mended that the chair be input lines IEC 61000 4 11 aaa nae powered from an uninter 30 dip in UT 80 dip in UT ruptible power supply or a for 25 cycles for 25 cycles battery lt O UT lt
12. g coun Pull up on the head rest to Firmly tighten the knob by turn ter clockwise expose the dowels ing clockwise to avoid slipping when in use DIRECTIONS FOR USE PROCEDURE TRAY USE C AUTI ON Make sure the Leg Rest is fully lowered before using the procedure tray Do not sit or push on the Procedure Tray when extended from the seat Maximum Weight rating of 15 lbs 6 8 kg Do not use the Procedure Tray when using the Trendelenburg function The Chair seat must remain flat while using the Procedure Tray Slide out the Procedure Tray by gare on the center slot of the tray holder until the tray stops After a procedure is performed remove the Procedure Tray with both hands at the side notches from the tray holder Discard fluids clean and place back into tray holder CLEANING AND DISINFECTING INSTRUCTIONS If fluid spill under the seat cushion follow these instructions 1 Remove the seat pad by pulling 2 Pull out the 2 pins on both sides 3 Unscrew the 4 black handles at up from the edge The pad is held of the metal plate near the end of the corners of the metal plate Slide on by Velcro the Procedure tray holder Slide the metal plate off from the seat the tray holder and Procedure section and disinfect all surfaces Tray out from the seat section FIXED T RAIL The Fixed T Rail can be on one or both sides of the seat section allowing the use of any t rail accessory with a Maximum Load Capacity of 150
13. hair SPECIFICATIONS PRODUCT SPECIFICATIONS Weight 280 325 Ibs 127 148 kg shipping Weight 372 417 lbs 169 189 kg Lifting Capacity 590 Ibs 250 kg ENVIRONMENTAL CONDITIONS Humidity Atmospheric Pressure 50 10 C to 104 40 C 20 to 60 RH 98 to 105 kPa storage amp Transport 20 29 C to 135 87 C 20 to 95 RH 98 to 105 kPa ELECTRICAL SPECIFICATIONS Designed for North America 120 VAC 15 amp 60 Hz 230 VAC 10 amp 50 60 Hz o 29amps Maximum Momentary 60 amos 3 0 amps Current Consumption i i Voltage Output to 24 VDC 24 VDC Actuators Electric Shock Tabletop Applied Part eel IN Type B Applied Part IN Type B Applied Part Ingress Protection Made of Operation Intermittent Operation Intermittent Operation MAX 2 minutes ON MAX 2 minutes ON 18 minutes off 18 minutes off Fuse Specifications M 10AL 125V M 10AL 125V SPECIFICATIONS Guidance and manufacturer s declaration electromagnetic emissions The chair is intended for use in the electromagnetic environment specified below The customer or the user of the chair should assure that it is used in such an environment Emissions Test Compliance Electromagnetic environment guidance The chair uses RF energy only for its internal RF emissions Group 1 function Therefore its RF emissions are very low CISPR 11 and are not likely to cause any interference in nearby electronic equipment CISPR 11 The chair is suitable for use in all esta
14. ions is important for the safety of the operator and patient The healthcare professional should read and understand this entire manual before use with a patient There are no known contradictions to the use of this equipment SYMBOL IDENTIFICATION This symbol when used in this manual and on product labels represents a caution warning Be sure to read and comply with all precautions and warnings This symbol when used in this manual and on product labels warns against an electrical shock hazard Be sure to observe and comply with all warnings This symbol when used in this manual or on product labels indicates a Protective Earth Ground Terminal This symbol when used in this manual or on product labels indicates that the product should be protected from moisture The humidity specifications for Transport amp Storage are listed in the environmental conditions section of this manual This symbol is used to indicate that the operator should consult the user manual This symbol when used in this manual and on product labels indicates that the table and com ponents are a Type B Applied Part pursuant to IEC 60601 1 2005 This symbol when used in this manual or on product labels indicates alternating current AC This symbol when used in this manual or on product labels indicates direct current DC A CAUTION READ AND SAVE THESE INSTRUCTIONS The Back Rest and Leg Rest sections are not designed to supp
15. ions on one or both sides of the back rest sec tion allowing the use of any t rail accessory Attach or remove using knobs The T Rail Adapter has a Maximum Load Capacity of 150 Ibs 68 kg POWER OUTLET USE A W ARN N G The maximum amperage for the Power Outlet is 3 amps Connecting equipment that exceeds this rating will damage the system Only connect low current devices Do not connect an extension cord or power strip to the Power Outlet Do not touch equipment connected to the Power Outlet and the patient at the same time Any electrical accessories used with this table must comply with approved medical standards Equipment relying only on Basic Insulation only one means of electrical protection for the patient pratitioner must not be used The Power Outlet can be used to connect low power devices such as localized illumination computers micro controllers etc Exceeding the maximum current will interrupt the power CLEANING amp DISINFECTION INSPECTIONS WARRANTY CLEANING amp DISINFECTION A W ARN NG Before cleaning with any liquid cleaner be sure to unplug the power cord from the outlet Use a 10 sodium hypochlorite bleach solution or Recommended Disinfectants on all surfaces Clean all sides of each upholstered section Follow the directions on the disinfectant and wipe off excess Recommended Disinfectants Protex MadaCide Accell TB Virox Note Damage caused by unapproved substances will not be
16. ll Holder 1 a L Self Adjusting Removable Arm Rests 2 accessory Fixed T Rail 2 option 7 S E iae gt Rotate up to 240 Swivel Base option STANDARD SPECIFICATIONS Powered 19 35 48 89 cm Height Range Powered 15 5 Trendelenburg Reverse Trendelenburg Motion 2 ica to 18 46 cm rolls 3 8 cm Comfort Foam OPTIONS Retractable Foot Pull out from under seat section fully Rests Stirrups adjustable Foot Control Supports all powered motions Fixed T Rail available on one or both sides of the seat Procedure Tray 12 25 x 10 25 31 x 26cm 2 qt 1 9 I 240 of rotation adds 1 5 4cm to height Swivel Base range amp 60 Ibs 27 kg to the weight Padding 4 10 cm Comfort Foam 4 4 Adjustable Head Rest accessory electric adjustment 0 to 80 Electric Retractable Foot Rests Stirrups 2 option electric adjustment 0 to 90 DN Electric Leg Rest Electric Lift Towers 2 Powered 0 80 Back Rest Powered 0 90 Leg Rest Hand Control All motions and memory function 3 Section Top 74 188cm long 80 203cm long with Head Rest extended x 27 69cm wide 26 long x 27 wide 66 x 69cm 22 5 long x 27 wide 57 x 69cm 13 long x 23 wide 33 x 58cm Ee Il long x 10 wide 28 x 25cm adjusting angle ACCESSORIES Adjustable Head Rest OR amp height remov
17. ort the entire weight of the patient Do not sit on the Back Rest ot Leg rest sections Medical Electrical Equipment needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided in this manual Portable and mobile RF communications equipment can affect Medical Electrical Equipment The use of accessories transducers and cables other than those specified by the manufacturer may result in increased emissions or decreased immunity of the Procedure Chair IMPORTANT SAFETY INSTRUCTIONS The arm rests are not designed to be used as patient restraints Use appropriate patient restraints The chair should not be used adjacent to or stacked with other equipment and that if adjacent or stacked use is necessary the chair should be observed to verify normal operation in the configuration in which it will be used The chair is designed to be a stand alone chair This chair must not be modified or incorporated into any other equipment As with any moving mechanism there are potential pinch points around and underneath the chair It is the responsibility of the operator of this equipment to insure that bystanders are not in the area below or around this equipment during operation Proper operation of this equipment is very important for the safety of the operator patient and any other individuals in the area of this equipment Directions for use of this equipment are described in thi
18. range P Interference may occur in the vicinity of equipment marked with the following symbol NOTE 1 At 80 MHz and 800 MHz 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 a 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 accura cy 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 chair is used exceeds the applicable RF com pliance level above the chair should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as re orienting or relocating the table b Over the frequency range 150 kHz to 80 MHz field strengths should be less than 1 V m REVISION HISTORY REVISION HISTORY DESCRIPTION 08 08 2013 Word New Document O B 08 21 2013 Updated to Indesign Format Updated specification section 01 27 2014 Added caution note to Procedure Tray section Updated Model Number Description Section 20
19. s manual The operator should read these sections carefully Weight Limit patient and accessories 550 Ibs 250 kg Do not exceed Be certain that the chair is completely lowered without any tilt being present prior to discharging an ambulatory patient The patient may lose balance and fall This chair is not suitable for use in the presence of flammable anesthetic mixture with air or oxygen or nitrous oxide When lowering the chair or using the Trendelenburg functions make sure there is nothing underneath the chair that can impede motion like stools cabinets accessory parts cleaners etc Use this furnishing only for its intended use as described in these instructions Do not use attachments not recommended by the manufacturer Close supervision is necessary when this furnishing is used near children or disabled persons The Oakworks Procedure Chair has two lifting columns that raise and lower the chair and three actuators that allow the client to be positioned for both client and therapist comfort Each of these devices has a duty cycle of approximately 10 meaning 2 minutes of operation within a 20 minute period Exceeding this duty cycle can damage the equipment Do not sit on the Backrest or Leg Rest A WARNING To reduce the risk of burns fire electric shock or injury to persons 1 Unplug this furnishing from the electrical outlet before cleaning 2 Unplug from outlet before adding or removing parts 3 Never operate
20. this furnishing if it has a damaged cord or plug if it is not working properly if it has been dropped or damaged or dropped into water Contact Oakworks Customer Service before use Keep the cord away from heated surfaces Never drop or insert any object into any opening Do not use outdoors Do not operate where aerosol spray products are being used or where oxygen is being administered oo ae ee PE The maximum amperage for the Power Outlet is 3 amps Connecting equipment that exceeds this rating will damage the system Only connect low current devices Do not connect an extension cord or power strip to the Power Outlet Do not touch equipment connected to the Power Outlet and the patient at the same time Any electrical accessories used with this table must comply with approved medical standards Equipment relying only on Basic Insulation only one means of electrical protection for the patient pratitioner must not be used A DANGER Risk of electric shock Connect this furnishing to a properly grounded outlet only See Grounding Instructions in this manual Electrical Shock Hazard The power supply control module is located under the chair seat No user serviceable parts are inside the control box Refer servicing to qualified personnel Unplug wall plug prior to contact with any cables connected to the power supply PRODUCT DESCRIPTION 300 Series Procedure Chair 12 Button p z Hand Control i aa 3 g Paper Ro
21. you use this button To set the chair into a different position simply follow steps above to readjust your memory position Memory Function DIRECTIONS FOR USE FOOT CONTROL OPERATIONS C AUTI ON Do not sit on the Fowler Backrest or Leg Rest sections Do not leave the patient unat tended When lowering the chair or using the Trendelenburg functions make sure there is nothing that can impede motion like stools cabinets accessory parts cleaners etc The Multi function Foot Control operates all functions by holding down one button at a time Follow the directions below to access these functions If a function button does not release pressing and holding any other function button will stop the motion The foot control has no memory positions Co Height Up Back Rest Up a Trendelenburg head end down up to 15 Y Reverse Trendelenburg foot end down up to 5 oF Height Down Back Rest Down DIRECTIONS FOR USE SWIVEL BASE USE A C AUTI O N When rotating the chair make sure there is nothing around the chair that can impede the rotational motion like stools cabinets etc Rotate up to 240 The chair can be rotated with a patient in it Locate the black push buttons at the top of the back rest section Press in and hold either one of the buttons to disengage the base locking mechanism While holding in the push button rotate the chair to the d
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