Graham Field Camping Equipment 765000 User's Manual
Contents
1. 8 765000 INS LAB RevC1 1 PUMP FRONT PANEL Front panel of pump is shown below Descriptions of buttons and indicators follow Auto Adjust button indicators at right of zo Therapy adjust button D S Qi POS Maxfirm button indicators at right of button ji ice indicat Paneliock button Service indicator indicator at right of button Power failure indicator Power ON OFF button indicator at right of button Low pressure OW Tuning button indicator 74 indicators at left of button Alarm mute button Front panel first row ie Auto Adjust button The auto adjust button adjusts the mattress pressure automatically based on the patient s weight To remind the user that the auto adjust process is ongoing the auto adjust indicator LEDs will periodically flash from left to right until the Ready LED illuminates to show the process is complete Three conditions trigger the auto adjust function 1 Press the auto adjust button for two seconds the mattress system automatically readjusts pressure setting 2 When initial mattress inflation is complete the mattress system automatically starts the auto adjust function 3 When the mattress system detects a significant change in patient s weight on the mattress e g patient egress or ingress the system automatically starts the auto adjust function When auto adjust is complete the Ready indicator will illuminate To disable the auto adjust function press the auto2. Info Provides application recommendations or other useful information to ensure that you get the most from your product DANGER To reduce the risk of electrocution DANGER Always unplug this product immediately after use N DANGER Do not use this product while bathing N DANGER Do not place or store this product where it can fall or be pulled into a tub or sink N DANGER Do not place this product in or drop into water or other liquid N DANGER Do not reach for a product that has fallen into water Unplug it immediately 4 765000 INS LAB RevC1 1 WARNING To reduce the risk of burns electrocution fire or personal injury N WARNING Do not leave this product unattended when plugged in N WARNING Always use close supervision when this product is used by on or near children or those who require close supervision N WARNING Use this product only as intended and described in this manual Do not use attachments or accessories not recommended by Graham Field N WARNING Never operate this product if a It has a damaged cord or plug b It is not working properly c It has been dropped or damaged d It has been dropped into water Return the product to your Graham Field equipment provider N WARNING Keep the cord away from heated surfaces N WARNING Never block the air openings of this product or place it on a soft surface such as a bed or couch where the openings may be blocked Keep the
3. Emissions Test Compliance Electromagnetic Environment Guidance Harmonic emissions Class A IEC61000 3 2 The device is suitable for use in all establishments including Voltage fluctuations domestic establishments and those directly connected to the Flicker emissions Complies public low voltage power supply network IEC61000 3 3 Guidance and Manufacturer s Declaration Electromagnetic Immunity This device is intended for use in the electromagnetic environment specified below The user of this device should make sure it is used in such an environment Electromagnetic Immunity Test IEC60601 test level Compliance Environment Guidance Floors should be wood concrete or Electrostatic a 6kV contact 6kV contact ceramic tile If floors are covered Discharge ESD i i 8kV air 8kV air with synthetic material the relative IEC61000 4 2 humidity should be at least 30 96 Electrical fast 2kV for power supply 2kV for power supply Mains power quality should be that transient burst line line of atypical commercial or hospital IEC61000 4 4 1KkV for input out line 1kV for input out line environment 1kV for differential t1kV for differential Mains power quality should be that mode mode of atypical commercial or hospital 2kV for common mode 2kV for common mode environment Surge IEC61000 4 5 Voltage dips 5 UT gt 95 dip in 5 UT gt 95 dip in Mains power quality should be that short UT for
4. LUNIEX A Graham Field Brand AltaDvne Sensor Plus 765000 ALTERNATING PRESSURE MATTRESS SYSTEM WITH ACTIVE SENSOR TECHNOLOGY USER MANUAL Important Do not operate the Mattress System without first reading and understanding this manual Save this manual for future use Info The most current version of this manual can he found online at www grahamfield com 765000 INS LAB RevC11 CONTENTS hugie deuge um e 3 INTENDED USE OF THIS DEVICE 420 3 CONTRAINDIGAT ION iiieanicacdenusuuzienecaudunuxi ud iras uiua iau a na 3 IMPORTANT SAFETY PRECAUTIONS creer 4 DANGER ee asser ee 4 RINE Ge een 5 IN Ee nc au 6 EQUIPMENT SYMBOLS cccccsssseecceeseecenenseeeenenseeeeneaseeeenneeeesenneseees 7 PRODUCT DESCRIPTION weicccssceepesescssncensensseceeseceetawacteesssnsventasivewccsseres 8 PUMP AND MATTRESS SYSTEM eene rennen 8 PUMP FHONT aa guo aua Da VEU Y vd a ce udin eaa nu sed nn 8 PUMP RER nes aies cada cR nn ed 8 PUMP FRONT PANEL 2 nan annmann teen aseemennn nanas EEEa 9 INSTALLATION a se te 13 UNPACRIN GS nissan een eE 13 PUMP AND MATTRESS SETUP eene rere 13 OPERATIONS t 15 GETTING STARTED 2 ees udine ies xus a tarda es ieee 15 QUICK DISCONNEG T nn ne a RE n aYRVaR CV aE 15 TRANSPORT CAD iccecccuivxes eccxEuuc ue Duke canne gus ac ike c
5. 0 5 cycle UT for 0 5 cycle of atypical commercial or hospital interruptions and 40 UT 60 dip in 40 UT 60 dip injenvironment If the user of this voltage UT for 5 cycles UT for 5 cycles device requires continued operation variations on 70 96 UT 30 9e dip in 70 UT 30 96 dip in during power mains interruptions it power supply UT for 25 cycles UT for 25 cycles is recommended that the device be input lines 5 UT 95 dip in 5 UT gt 95 dip inipowered from an uninterruptible IEC61000 4 11 UT for 5 sec UT for 5 sec power supply or a battery Power frequency Power frequency magnetic fields 50 60Hz should be at levels characteristic of magnetic field atypical location in a typical IEC61000 4 8 commercial or hospital environment NOTE U is the a c mains voltage prior to the application of the test level 765000 INS LAB RevC1 1 21 Guidance and Manufacturer s Declaration Electromagnetic Immunity This device is intended for use in the electromagnetic environment specified below The user of this device should make sure it is used in such an environment IEC60601 test C li Electromagnetic level pets Environment Guidance Portable and mobile RF communications equipment Immunity Test should be used no closer to any part of this device including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Conducted RF 3Vrms150 kHz to Recommend
6. ErvEE up kir ca Eurer 16 CPR FUNCTION Sn cds 16 MAINTENANCE ee us 17 CANIN tstesie eels end se EEEE EEEE EEEE EEEE 17 GENERAL MAINTENANCE 00 ccccsssesceeeeeeeeeeeeeeeeeeeeeeeeeeseeeeeeeeeeeneees 17 FUSE HEPLACEMENI iuad iine srida usua a cus cud soto n Daun as iE utn rra ducum 18 AIR FILTER REPLACEMEND iiic ccxon isnt YkEuE S cnn on haa xau ES da naua ad E no 18 STORA OE 18 jx elgewie lm 8 19 LIMITED WARRANTY sssixkkkskxitawEakEEPA NICHE YID OU EX EIRNE E EEXOKUXA EN KE KE IPEE YER 20 APPENDIX A EMC INFORMATION eere eneneee nnn 21 Graham Field Lumex and AltaDyne are registered trademarks of GF Health Products Inc GF Health Products Inc Graham Field is not responsible for typographical errors Packaging warranties specifications and products are subject to change without notice 2 765000 INS LAB RevC1 1 INTRODUCTION Use this manual for set up and operation of the Lumex AltaDyne Sensor Plus 765000 Alternating Pressure Mattress System with Active Sensor Technology Read all instructions before using the mattress system Save this manual for future reference INTENDED USE OF THIS DEVICE The intended use of the Lumex AltaDyne Sensor Plus 765000 Alternating Pressure Mattress System with Active Sensor Technology is e Aid in the treatment and prevention
7. MHz to 2 5 GHz W d 12VP d 1 2VP d 2 E 0 28 o 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 765000 INS LAB RevC11 23 USA Corporate Headquarters GF Health Products Inc 2935 Northeast Parkway Atlanta Georgia 30360 telephone 770 368 4700 fax 770 368 2386 GRAHAM FIELD www grahamfield com 2011 GF Health Products Inc
8. PANEL for a complete description of available adjustments buttons and indicators QUICK DISCONNECT Pull the power plug from the wall connector to disconnect the device quickly 765000 INS LAB RevC11 15 TRANSPORT CAP In case of power failure or quick connector transport Disconnect the quick n connector and cap the mattress with the transport cap to slow deflation Info This system is equipped with cell on cell technology to provide added support and prevent sco cap bottoming out in the event of a power failure Lower cells will hold air for approximately eight hours CPR FUNCTION If CPR must be performed on the patient while the mattress is in use to immediately deflate the mattress either 1 Pull the CPR valves from the mattress in the location of the arrow shown at right or 2 Disconnect the quick connector from the pump in the location of the arrow shown at right 16 765000 INS LAB RevC11 MAINTENANCE CLEANING WARNING To reduce the risk of increased bacterial growth infection illness or injury from contamination thoroughly clean and dry the mattress system before use and as necessary during use as follows Pump Wipe the pump with a clean damp cloth and mild detergent and keep it away from dust Air dry A NOTICE Do not use phenolic products or corrosive or powdered cleansers to clean the pump A NOTICE Do not immerse or soak the pump Mattress Wipe the mattress unit with a cl
9. adjust button until auto adjust indicators de illuminate Info During the auto adjust operation it is normal for the mattress system to cycle through a series of inflation and deflation 765000 INS LAB RevC1 1 9 eet gt Tuning button The tuning button fine tunes the mattress system s auto adjusted pressure Three tuning settings are available 0 System auto adjusted pressure One level softer than auto adjusted pressure One level firmer than auto adjusted pressure Info The tuning function ts only available in alternate and static therapy modes Front panel second row Qe Therapy adjust button The therapy adjust button selects the therapy mode After power up the system automatically inflates the mattress auto adjusts the pressure and enters alternate therapy mode To then cycle among the therapy settings press the therapy adjust button to select static therapy mode press again to select alternate seat inflation therapy mode press again to select static seat inflation therapy mode press again to select alternate therapy mode etc Alternate Each tube fills for 10 minutes then deflates for 10 minutes alternately to the next tube When selected the alternate indicator illuminates Static The pressure inside all tubes is adjusted to the same pressure When selected the static indicator illuminates Alternate Seat Inflation For use when the head is raised to increase pr
10. air opening free of lint hair and other similar particles N WARNING Never drop or insert any object into any opening or hose N WARNING Connect this product only to a properly grounded power outlet N WARNING Maximum patient weight capacity for this product is 400 Ib 189 kg 765000 INS LAB RevC1 1 5 N WARNING Patient entrapment with bed side rails may cause injury or death The bed frame and its components including the mattress bed side rails head and foot board bedding and any accessories added to the bed can all affect the risk of entrapment Thorough patient assessment and monitoring are necessary to reduce the risk of entrapment including establishing whether the use of a bed rail is in the best interest of the patient Read and understand the User Manual before using this equipment GF Health Products Inc product manuals are available online at www grahamfield com Visit the FDA s Bed Safety page at www fda gov to learn more about the risks of entrapment It is the responsibility of the facility and provider to be in compliance with these guidelines Refer to user manuals for beds and rails for additional product safety information After any adjustment repair or service and before use ensure all attaching hardware is securely tightened Bed rails with dimensions different than the original equipment specified by the bed manufacturer may not be interchangeable and may result in entrapment or other inj
11. ance for transmitters in these frequency ranges c 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 device is used exceeds the applicable RF compliance level above the device should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as reorienting or relocating the device d Over the frequency range 150 kHz to 80 MHz field strengths should be less than 3 V m Recommended separation distances between portable and mobile RF communications equipment and this device This device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled The customer or the user of this device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and this device as recommended below according to the maximum output power of the communications equipment Rated maximum Separation distance according to frequency of transmitter m output power of transmitter 150 kHz to 80 MHz 80 MHz to 800 MHz 800
12. d with ground properly wired in good electrical condition and keep it as short as possible N WARNING Ensure that the local power voltage is appropriate for the pump unit 5 Plug the power cord into a properly grounded electrical outlet 14 765000 INS LAB RevC1 1 OPERATION GETTING STARTED 1 Turn the main power switch man to the ON position SUR 2 Press the front panel power D uo button The power indicator Orem O e e e 8 Q Q n will illuminate power button Info The mattress system will automatically enter maxfirm mode for the quickest inflation at set up when inflated it will then automatically enter auto adjust mode to select the appropriate pressure 3 The pump will begin delivering air into the mattress The low pressure indicator and the maxfirm indicator will illuminate for approximately twenty minutes until the mattress is fully inflated 4 Upon inflation the system will automatically enter auto adjust mode to automatically select the appropriate pressure according to the patient s weight The auto adjust indicator LEDs will flash from left to right and the system will cycle through inflation and deflation until the Ready LED illuminates to show the process is complete and the mattress system automatically enters alternate therapy mode 5 Replace all sheets blankets and pillows on the bed 6 You can now adjust therapy modes or tuning Please see earlier section PUMP FRONT
13. e of pump previously shown in PUMP REAR must be ON in order for the front panel power button to function Alarm Mute button The alarm mute button temporarily suspends the LED indicator and buzzer when either the low pressure alarm or power failure alarm is activated Should the problem not be resolved within three minutes the alarm will resume 765000 INS LAB RevC11 11 low Pressure Low pressure indicator The low pressure indicator yellow LED illuminates and the alarm sounds when an abnormally low pressure level occurs If the low pressure indicator persistently illuminates inappropriately 1 Check to ensure all connections are properly and securely connected per installation instructions 2 Check for any leakage tubes or connecting hoses If necessary contact your Graham Field equipment provider to replace any damaged tubes or hoses 3 If problem persists contact your Graham Field equipment provider Info Sometimes the low pressure indicator will illuminate when a patient gets up to leave the bed This is normal The indicator will turn off automatically after a short time The low pressure indicator will illuminate until the low pressure condition is resolved C PowerFailure Power failure indicator The power failure indicator illuminates and the alarm sounds when there is a power failure Depress the alarm mute button to disable both alarm and LED Service Service indicator Mechanical failu
14. ean damp cloth and mild detergent The mattress may also be cleaned using a 1076 solution of sodium hypochlorite bleach diluted in water Air dry all parts thoroughly before use A NOTICE Do not use phenolic products to clean the mattress A NOTICE After cleaning air dry the mattress without direct exposure to sunlight GENERAL MAINTENANCE 1 Check main power cord for abrasion or excessive wear 2 Check mattress cover for signs of wear or damage Ensure mattress cover and tubes are connected correctly 3 Check airflow from the air hose connector The airflow should alternate between each connector every half cycle time while in alternating mode 4 Checkthe air hoses for any kink or break For replacement please contact your GF equipment provider 765000 INS LAB RevC1 1 17 Fuse replacement If you suspect a blown fuse Use a small screwdriver to remove tool needed small screwdriver disconnect the plug from the wall outlet immediately the cover of the fuse holder fuse locations are shown in picture at right Insert a new fuse of the correct rating T1A 250V VDE approved Replace the fuse holder cover Ensure that fuse holder cover is securely installed Air filter replacement tool needed small screwdriver 1 Usea small screwdriver to remove the air filter plate located at rear of pump filter location is shown in picture at right 2 Remove the filter The filter is reu
15. ed separation IEC 61000 4 6 80 MHz outside distance ISM bands d 1 2VP 150kHz to 80MHz Radiated RF 3 V m 80 MHz to 3V m IEC 61000 4 3 d 124 P 150kHz to 80MHz d 2 34 P 80 MHz to 2 5G MHz Where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer and d is the recommended separation distance in meters m Field strengths from fixed RF transmitters as determined by an electromagnetic site survey should be less than the compliance level in each frequency range Interference may occur in the vicinity of equipment marked with the following symbol Co 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 22 765000 INS LAB RevC11 a The ISM industrial scientific and medical bands between 150 kHz and 80 MHz are 6 765 MHz to 6 795 MHz 13 553 MHz to 13 567 MHz 26 957 MHz to 27 283 MHz and 40 66 MHz to 40 70 MHz b The compliance levels in the ISM frequency bands between 150 kHz and 80 MHz and in the frequency range 80 MHz to 2 5 GHz are intended to decrease the likelihood that mobile portable communications equipment could cause interference if it is inadvertently brought into patient areas For this reason an additional factor of 10 3 is used in calculating the recommended separation dist
16. essure under the buttocks in alternating pressure therapy mode When selected both the alternate and seat inflation indicators illuminate Static Seat Inflation For use when the head is raised to increase pressure under the buttocks in static therapy mode When selected both the static and seat inflation indicators illuminate 10 765000 INS LAB RevC1 1 Q Maxfirm button The pump will automatically enter maxfirm mode every time the power is turned on Maxfirm mode ensures the pump is able to reach its maximum operating pressure Maxfirm mode will last for 20 minutes and then the system will automatically enter auto adjust mode To disable maxfirm mode press the maxfirm button When enabled the maxfirm indicator at left of button illuminates Front panel third row Q s Panel lock button The panel lock button sets the panel lock to protect the panel settings from accidental change Press for two seconds to lock press FIRMLY for two seconds to unlock After the panel has been untouched for five minutes the panel lock locks automatically When the panel is locked the panel lock indicator will illuminate OQ Power ON OFF button The power button turns power to the mattress system ON or OFF Press to turn ON press to turn OFF When power is on the power ON OFF indicator will illuminate When power is turned OFF the mattress system will slowly deflate Info Main power switch on sid
17. ifications are subject to change without notice 765000 INS LAB RevC11 19 LIMITED WARRANTY GF Health Products Inc warrants the Lumex AltaDyne Sensor Plus 765000 Alternating Pressure Mattress System with Active Sensor Technology for a period of twelve months for defects in workmanship and materials If a product is deemed to be under warranty GF Health Products Inc shall provide at its option 1 replacement of any defective part or product or 2 a credit of the original selling price made to GF Health Products Inc s initial customer The warranty does not include any labor charges incurred in replacement part s installation or any associated freight or shipping charges to GF Health Products Inc The warranties contained herein contain all the representations and warranties with respect to the subject matter of this document and supersede all prior negotiations agreements and understandings with respect thereto The recipient of this document hereby acknowledges and represents that it has not relied on any representation assertion guarantee warranty collateral contract or other assurance except those set out in this document 20 765000 INS LAB RevC11 APPENDIX A EMC INFORMATION Guidance and Manufacturer s Declaration Electromagnetic Emissions This device is intended for use in the electromagnetic environment specified below The user of this device should make sure it is used in such an environment
18. of stage 1 2 3 and 4 pressure ulcers while optimizing user comfort e Pain management as prescribed by a physician e As described above in either a homecare or long term care setting Contraindication N WARNING DO NOT use this product in the presence of flammable anesthesia There is a possible fire hazard when this product is used with certain oxygen delivery equipment Use nasal cannula face mask or 1 2 length oxygen tent to deliver oxygen in the presence of this product DO NOT use a full length oxygen tent that extends past the top surface of the mattress with this product 765000 INS LAB RevC1 1 3 IMPORTANT SAFETY PRECAUTIONS The safety statements presented in this chapter refer to the basic safety information that should be observed by those using this Mattress System There are additional safety statements in other chapters or sections which may be the same as or similar to the following or specific to the operations N DANGER Indicates an imminent hazard situation that if not avoided will result in death or serious injury N WARNING Indicates a potential hazard situation or unsafe practice that if not avoided could result in death or serious injury N CAUTION Indicates a potential hazard or unsafe practice that if not avoided could result in minor or moderate personal injury A NOTICE Indicates a potential hazard or unsafe practice that if not avoided could result in product or property damage
19. re service required contact your Graham Field equipment provider 12 765000 INS LAB RevC11 INSTALLATION UNPACKING 1 Carefully remove all components from the carton 2 Inspect all components 3 If damage is evident to the contents please notify the carrier and your Graham Field equipment provider PUMP AND MATTRESS SETUP 1 Place the mattress on top of the bed frame ensure that the foot end symbol faces up at foot end as shown at right Secure mattress to bed with straps 2 Fold open the wire hangers on the back of the pump as shown at right 3 Either hang the pump on the bed s foot end as shown at right or place the pump on a flat surface easily accessible to the caregiver and or doctor A NOTICE Place the device ina position where the caregiver and or doctor can access it easily 4 Connect the mattress pump air hose quick connector ensure that the connector has clicked securely into place before continuing A NOTICE Ensure that the air hoses are not kinked or tucked under the mattress 765000 INS LAB RevC11 13 N WARNING Locate all cords so that they will not be stepped on tripped over or otherwise subjected to damage or stress N WARNING Do not use a household extension cord if the electrical cord does not reach the power outlet Use of an improper extension cord could result in fire and electric shock If an extension cord must be used use a three conductor cor
20. sable if not torn and can DE be washed gently with a mild detergent and water Dry the filter before use 3 Replace the filter and cover Ensure that filter cover is securely installed Replace the air filter regularly if it is gray torn or the environment is dirty STORAGE 1 Lay the mattress out flat and upside down 2 Roll from the head end toward the foot end 3 Stretch the foot end strap around the rolled mattress to prevent unrolling 4 Store mattress and pump in a dust free environment with no exposure to direct sunlight A NOTICE Do not fold crease or stack the mattress 18 765000 INS LAB RevC11 SPECIFICATIONS label on product Specification Power Supply Info see rating AC 120V 60 Hz 0 17A for 120V system Fuse Rating Cycle time Dimensions L x W x H Environment Temperature Humidity Classification T1A 250V Fixed 10 minutes 11 4 x 7 9 x 4 6 29 1 x 20 x 11 7 cm Operation 50 F to 104 F 10 C to 40 C Storage 5 F to 122 F 15 C to 50 C Shipping 5 F to 158 F 15 C to 70 C Operation 10 to 90 non condensing Storage 10 to 90 non condensing Shipping 10 to 90 non condensing Class II with functional earth Type BF IPX0 Applied Part Air Mattress Not suitable for use in the presence of a flammable anesthetic mixture No AP or APG protection Mattress Specification Dimensions L x W x H 78 7 x 35 4 x 8 200 x 90 x 20 3 cm Info Spec
21. ury NOTICE A NOTICE The pump can be used only with the accompanying mattress Do not use it for any other purpose 6 765000 INS LAB RevC1 1 EQUIPMENT SYMBOLS Manufacturer BF symbol Indicates that this product is in accordance with the degree of protection against electric shock for type BF equipment Functional earth for UL only Attention Read the instructions Disposal of Electrical amp Electronic Equipment WEEE Do not treat this product as household waste For more detailed information with regard to returning and recycling this product please consult your local city office household waste disposal service or Graham Field equipment provider i Consult operating instructions n Class Il for UL only The system has been tested and successfully approved with the following standards C C EN 60601 1 EN 60601 1 2 EN 550011 Class B IEC61000 3 2 IEC61000 3 3 0197 For U S and Canada only Medical Equipment Air Pump E228589 with respect to electrical shock fire and 53DG mechanical hazards only in accordance with UL60601 1 and CAN CSA C22 2 No 601 1 765000 INS LAB RevC1 1 7 PRODUCT DESCRIPTION PUMP AND MATTRESS SYSTEM foot end symbol CPR valves mattress i pump quick connectors mattress pump connectors pump and mattress system PUMP FRONT gt Mick connector PUMP REAR main power switch hanger power cord receptacle filter
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