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1. This device is intended for use in an electromagnetic environment in which radiated RF disturbances ar 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 MHz to 2 5 GHz For transmitters rated at a maximum output power not listed above the recommended separation distance din 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 765000S INS LAB RevC14 27 Manufactured for GF Health Products Inc 2935 Northeast Parkway Atlanta Georgia 30360 telephone 770 368 4700 fax 770 368 2386 GRAHAM FIELD www grahamfield com 2013 GF Health Products Inc Made in Taiwan2. 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 Check the air hoses for any kink or break For replacement please contact your Graham Field authorized distributor 20 765000S INS LAB RevC14 Fuse replacement tool needed small screwdriver 1 If you suspect a blown fuse disconnect the plug from the wall outlet immediately fuse 2 Use a small screwdriver to remove the cover of the fuse holder fuse locations are shown in picture at right 3 Insert a new fuse of the correct rating T1A 250V VDE approved 4 Replace the fuse holder cover Ensure that fuse holder cover is securely installed Air filter replacement tool needed small screwdriver 1 Use a small screwdriver to remove the air filter plate located at rear of pump filter location is shown in picture at right filter 2 Remove the filter The filter is reusable if not torn and can be washed gently with a mild detergent and water Dry the filter
3. purpose 765000S INS LAB RevC14 7 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 authorized distributor Consult operating instructions Class Il for UL only The system has been tested and successfully approved with the following standards C EN 60601 1 EN 60601 1 2 EN 550011 Class B IEC61000 3 2 IEC61000 3 3 For U S and Canada only Medical Equipment Air Pump E305034 UL with respect to electrical shock fire and 53DG mechanical hazards only in accordance with UL60601 1 and CAN CSA C22 2 No 601 1 8 765000S INS LAB RevC14 PRODUCT DESCRIPTION PUMP AND MATTRESS SYSTEM foot end symbol CPR valves mattress k J i pump quick connectors mattress pump connectors pump and mattress system 765000S INS LAB RevC14 PUMP FRONT Mick connector PUMP REAR switch power cord receptacle filter 10 765000S INS LAB RevC14 PUMP FRONT PANEL Front panel of pump is shown below Descriptions of buttons and indicators foll
4. 5 CLINICAL CARE 765000 Not made with natural rubber latex CLINICAL PLUS 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 be found online at www grahamfield com 765000S INS LAB RevG14 CONTENTS INTRODUCTION Aa EEEREN SEESE 3 INTENDED USE OF iaiia 3 CONTRAINDICATION 3 IMPORTANT SAFETY PRECAUTIONS cccccccsssssesseeeeeeeeeeeeeenneesseeseeeeeeseeenanenees 4 DANGEE access 5 oA a cidade cede sutuisasanveeisecensaseutsvetsausedeucse 6 ASALE E E E E E 7 EQUIPMENT 8 PRODUCT DESCRIP TION 9 PUMP AND MATTRESS SYSTEM ccccccssssseesseeeeeeeeeeeeeeneeeseeseeeeeeeeennnenees 9 PUMP i ae E a aR 10 ented auuedechstusthuvecenusussuadeaddeaiubeectsensase 10 PUMP FRONT PANEL 11 INSTALLATION 15 15 PUMANMDAIRESSO naina naana 16 OPERATION S EES aaRS 18 GETTING STARTED asisip cane cetabstenciantetaeuencecneetdsanneessecwsetessustens 18 18 TRANSPORT CGAP osanaan Eaa Eara 19 19 20 20 GENERBAMANIFENMNMNCEfCFFFFF 20 PUSE REPLACEMEN 21 AIR FILTER REPLACE MEN 21 SJEO STATE AE 21 TROUBLESHOOTING ices desioei 22 Od Sane 22 SPECIFICATIONS e 23 ONE 1 YEAR LIMITED WARRANTY 24 APPENDIX A EMC INFORMAIIOM 25 SIMMONS Clinical Care products manufactured by GF Health Products
5. 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 765000S INS LAB RevC14 21 TROUBLESHOOTING Problem Solution Power is not ON Ensure the plug is connected to a power source e Check if fuse is blown Alarm is on e Check if power has suddenly shut off Audible amp visible Ensure the CPR is sealed Ensure connection between air tube connector and pump unit is secure Ensure all tubing connections along mattress are secure Patient is bottoming Pressure setting might be inadequate for out patient adjust comfort range one to two levels higher and wait a few minutes for maximum comfort Mattress form is loose Ensure all snap buttons and mattress straps are securely fastened Ensure mattress is fixed to bed frame by straps No air produced from This is normal since there is alternating mode some air outlets of the Air outlets take turns to produce air during their air tube connector cycle time If the problem still occurs contact your Graha
6. 14 A WARNING Ensure that the local power voltage is appropriate for the pump unit 5 Plug the power cord into a properly grounded electrical outlet 765000S INS LAB RevC14 17 OPERATION GETTING STARTED 1 Turn the main power switch main4 to the ON position Laer ar 2 Press the front panel power button The power indicator 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 PANEL for a complete description of available adjustments buttons and indicators QUICK DISCONNECT Pull the pow
7. 1kV for input out 1kV for input out line line 2kV for power Mains power quality should be that of a typical commercial or hospital environment Electrical fast transient burst IEC61000 4 4 1 kV line s to 1 kV line s to Mains power quality should be that of a typical commercial or hospital environment Surge line s IEC61000 4 5 2 kV line s to earth line s Voltage dips short interruptions and voltage variations on power supply input lines IEC61000 4 11 Power frequency 50 60Hz magnetic field IEC61000 4 8 lt 5 Ur gt 95 dip in U for 0 5 cycle 40 U 60 dip in U for 5 cycles 70 U 30 dip in Ur for 25 cycles lt 5 Ur gt 95 dip in Ur for 5 sec lt 5 Ur gt 95 dip in Ur for 0 5 cycle 40 U 60 dip in Ut for 5 cycles 70 U 30 dip in Ur for 25 cycles lt 5 Ur gt 95 dip in Ur for 5 sec NOTE U is the a c mains voltage prior to the application of the test level 765000S INS LAB RevC14 Mains power quality should be that of a typical commercial or hospital environment If the user of this device requires continued operation during power mains interruptions it is recommended that the device be powered from an uninterruptible power supply or a battery Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment 25 Guidance and Manufacturer s
8. 5000S INS LAB RevC14 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 Emissions Test Compliance Electromagnetic Environment Guidance Group1 The device uses RF energy only for its internal function Therefore its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment RF emissions Class B CISPR 11 RF emissions CISPR 11 Harmonic emissions Cesa fre device is suitable for use in all establishments including IEC61000 3 2 domestic establishments and those directly connected to the Voltage fluctuations public low voltage power supply network Flicker emissions Complies 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 IEC60601 Test Level Electromagnetic Immunity Test Environment Guidance Compliance Floors should be wood concrete or ceramic tile If floors are covered with synthetic material the relative humidity should be at least 30 6kV contact 8kV air 6kV contact 8kV air Electrostatic Discharge ESD IEC61000 4 2 2kV for power supply line supply line
9. 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 Immunity Test IEC60601 test level Compliance Electromagnetic Environment Guidance Portable and mobile RF communications equipment should be used no closer to any part of this device including cables than there commended separation distance calculated from the equation applicable to the frequency of the transmitter Recommended separation distance d 1 2VP 150kHz to 80MHz d 1 2VP 150kHz to 80MHz d 2 3 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 MHz outside ISM as determined by an electromagnetic site bande survey should be less than the IEC 61000 4 6 compliance level in each frequency range 3Vrmsi50 kHz to 80 Radiated RF Interference may occur in the vicinity of 3 V m 80 MHz to 2 5 equipment marked with the following IEC 61000 4 3 GHz 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 a The ISM industrial scientific and
10. Inc under license from the trademark owner Dreamwell Ltd a subsidiary of Simmons Bedding Company Atlanta Georgia SIMMONS is a trademark of Dreamwell Ltd a subsidiary of Simmons Bedding Company 2013 Dreamwell Ltd All rights reserved Graham Field is a registered trademark of GF Health Products Inc GF Health Products Inc is not responsible for typographical errors All illustrations specifications packaging and warranties contained in this catalog are based on the latest product information available at the time of printing The most current product information can be found online at www grahamfield com 2 765000S INS LAB RevC14 INTRODUCTION Use this manual for set up and operation of the SIMMONS Clinical Care 765000S Clinical Plus 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 SIMMONS Clinical Care 765000S Clinical Plus Alternating Pressure Mattress System with Active Sensor Technology is e Aid in the treatment of 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 Z WARNING DO NOT use this product in the presence of flammable anesthesia There is a possible fire hazard when this product is used with
11. LLATION 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 authorized distributor 765000S INS LAB RevC14 15 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 the air hoses are not kinked or tucked under the mattress A WARNING Locate all cords so that they will not be stepped on tripped over or otherwise subjected to damage or stress A 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 cord with ground properly wired in good electrical condition and keep it as short as possible 16 765000S INS LAB RevC
12. PAIR OR REPLACEMENT OF THE DEFECTIVE PARTS GF SHALL NOT BE LIABLE FOR AND HEREBY DISCLAIMS ANY DIRECT SPECIAL INDIRECT INCIDENTAL EXEMPLARY OR CONSEQUENTIAL DAMAGES INCLUDING BUT NOT LIMITED TO DAMAGES FOR LOSS OF PROFITS OR INCOME LOSS OF USE DOWNTIME COVER OR EMPLOYEE OR INDEPENDENT CONTRACTOR WAGES PAYMENTS AND BENEFITS 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 For additional information on this product or this warranty please contact a GF Customer Service Representative NOTES 1 Additional terms and conditions may apply 2 Freight claims must be notated on the Bill of Lading and must be made with immediacy The ICC regulations govern specific requirements for freight claims Failure to abide by those regulations may result in a denial of the freight claim GF will assist you in filing the freight claim 3 Claims for any short shipment must be made within thirty 30 days of the invoice date GF Health Products Inc 2935 Northeast Parkway Atlanta GA 30360 Tel 770 368 4700 Fax 770 368 2386 www grahamfield com 24 76
13. RNING Notice for California Customers California Proposition 65 WARNING This product contains a chemical known to the State of California to cause cancer and reproductive or developmental harm 6 765000S INS LAB RevC14 A 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 Graham Field 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 injury NOTICE A NOTICE The pump can be used only with the accompanying mattress Do not use it for any other
14. 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 765000S INS LAB RevC14 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 DANGER Indicates an imminent hazard situation that if not avoided will result in death or serious injury Z WARNING Indicates a potential hazard situation or unsafe practice that if not avoided could result in death or serious injury Z 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 Info Provides application recommendations or other useful information to ensure that you get the most from your product 4 765000S INS LAB RevC14 DANGER To reduce the risk of electrocution DANGER Always unplug this product immediately after use M DANGER Do not use this product while bathing Z DANGER Do not place or st
15. er plug from the wall connector to disconnect the device quickly 18 765000S INS LAB RevC14 TRANSPORT CAP In case of power failure or quick connector transport Disconnect the quick 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 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 765000S INS LAB RevC14 19 MAINTENANCE CLEANING A 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 clean damp cloth and mild detergent The mattress may also be cleaned using a 10 solution of sodium hypochlorite
16. m Field authorized distributor SERVICE If a problem occurs with the SIMMONS Clinical Care 765000S Clinical Plus Alternating Pressure Mattress System with Active Sensor Technology that you are unable to resolve contact your Graham Field authorized distributor for service 22 765000S INS LAB RevC14 SPECIFICATIONS Power Supply Info see rating label on product 52d Environment Temperature 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 Humidity Operation 10 to 90 non condensing Storage 10 to 90 non condensing Shipping 10 to 90 non condensing Classification 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 Specification Dimensions L x W x H 78 7 x 35 4 x 8 200 x 90 x 20 3 cm 765000S INS LAB RevC14 23 ONE 1 YEAR LIMITED WARRANTY SCOPE OF WARRANTY GF Health Products Inc GF warrants to the original purchaser only that it will replace or repair components at GF s sole discretion that are defective in material or workmanship under normal use and service All warranties are conditioned upon the proper use of the products strictly in accordance with good commercial practice and applicable GF instructions and manuals including proper use and maintenance To the extent that a com
17. 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 distance for transmitters in these frequency ranges 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 26 765000S INS LAB RevC14 Recommended separation distances between portable and mobile RF communications equipment and this device
18. n accident freight damage tampering or failure to seek and obtain repair or replacement in a timely manner 2 Products which are not installed used or properly cleaned and maintained as required in the official manual for the applicable product 3 Products considered to be of a non durable nature including but not limited to casters filters fuses gaskets lubricants and charts 4 Accessories or parts not provided by GF 5 Charges by anyone for adjustments repairs replacement parts installation or other work performed upon or in connection with such products which are not expressly authorized in writing in advance by GF 6 Any labor or shipping charges incurred in the replacement part installation or repair 7 Costs and expenses of regular maintenance and cleaning and 8 Representations and warranties made by any person or entity other than GF ENTIRE WARRANTY EXCLUSIVE REMEDY AND CONSEQUENTIAL DAMAGES DISCLAIMER THIS WARRANTY IS GF S ONLY WARRANTY AND IS IN LIEU OF ALL OTHER WARRANTIES EXPRESS OR IMPLIED GF MAKES NO IMPLIED WARRANTIES OF ANY KIND INCLUDING ANY IMPLIED WARRANTIES OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE IF ANY MODEL OR SAMPLE WAS SHOWN TO THE CUSTOMER SUCH MODEL OR SAMPLE WAS USED MERELY TO ILLUSTRATE THE GENERAL TYPE AND QUALITY OF THE PRODUCT AND NOT TO REPRESENT THAT THE PRODUCT WOULD NECESSARILY CONFORM TO THE MODEL OR SAMPLE IN ALL RESPECTS THIS WARRANTY IS LIMITED TO THE RE
19. ore this product where it can fall or be pulled into a tub or sink Z DANGER Do not place this product in or drop into water or other liquid DANGER Do not reach for a product that has fallen into water Unplug it immediately 765000S INS LAB RevC14 WARNING To reduce the risk of burns electrocution fire or personal injury A WARNING Use this product only as intended and described in this manual Do not use attachments or accessories not recommended by Graham Field Z WARNING Do not leave this product unattended when plugged in WARNING Always use close supervision when this product is used by on or near children or those who require close supervision A A WARNING Never operate this product if a it has a damaged cord or plug b itis not working properly c it has been dropped or damaged or d it has been dropped into water Return the product to your Graham Field authorized distributor A WARNING Keep the cord away from heated surfaces A A 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 air opening free of lint hair and other similar particles A WARNING Never drop or insert any object into any opening or hose A WARNING Connect this product only to a properly grounded power outlet A WARNING Maximum patient weight capacity for this product is 400 Ib 189 kg EVENLY DISTRIBUTED A WA
20. ow ator Auto Adjust button indicators at right of ae 0 Static ieee MaxFirm Ss Therapy adjust button Q Maxfirm button indicators at right of button ji Service indicator Panel lock button indicator at right of button Power failure indicator Low pressure indic Tuning button indicators at left of button Power ON OFF button Alarm mute button indicator at right of button Front panel first row eo 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 auto adjust button until auto adjust indicators de illuminate Info During the auto adjust operation it i
21. ponent is warranted by a third party GF conveys all of its rights under that warranty to the original purchaser to the extent permitted This limited warranty shall only apply to defects that are reported to GF s customer service team within the applicable warranty period and which upon examination by GF or its authorized representative prove to be a warranty item This limited warranty is not transferable The warranted components and time period are set forth below SIMMONS Clinical Care 765000S Clinical Plus Alternating Pressure Mattress System with Active Sensor Technology one year The applicable warranty period shall commence from date of shipment to the original customer unless there is an expiration date on the component in which case the warranty shall expire on the earlier of warranty period or the expiration date OBTAINING WARRANTY SERVICE A GF Customer Service Representative must authorize warranty service Please contact the GF Customer Service department by calling 678 291 3207 sending a fax request to 770 368 2386 or by e mailing a request to cs grahamfield com Specific directions will be provided by the Customer Service Representative Failure to abide by the specific directions will result in denial of the warranty claim EXCLUSIONS The warranty does not cover and GF shall not be liable for the following 1 Defects damage or other conditions caused in whole or in part by misuse abuse negligence alteratio
22. s normal for the mattress system to cycle through a series of inflation and deflation 765000S INS LAB RevC14 11 ae vue 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 is only available in alternate and static therapy modes Front panel second row gt a 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 pressure under the buttocks in alternating pressure therapy mode When selected both the alternate and seat infla
23. tion 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 12 765000S INS LAB RevC14 a 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 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 i 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 side of pump previously shown in PUMP REAR must be ON in order for the front panel power button to function Alarm Mute b
24. utton 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 765000S INS LAB RevC14 13 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 authorized distributor to replace any damaged tubes or hoses 3 If problem persists contact your Graham Field authorized distributor 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 Powerralure_ 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 failure service required contact your Graham Field authorized distributor 14 765000S INS LAB RevC14 INSTA
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