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1. every other tube fills then deflates Static all tubes remain full and Seat Inflation when the head is raised to increase pressure under the buttocks Press the therapy adjust button at the left end of the row to cycle between the settings The selected therapy mode setting s indicator will illuminate 760000S INS LAB RevC14 9 Front panel fourth row Panel lock button The panel lock protects the panel settings from accidental change Press for two seconds to lock press for two seconds to unlock When the panel is locked the panel lock indicator will illuminate Power button ON OFF The power button turns power to the mattress 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 mattress will slowly deflate Info Main power switch on side of pump must be ON in order for the 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 five minutes the alarm will resume Low pressure indicator The low pressure indicator illuminates and the alarm sounds when the pressure level is lower than the selected pressure If the low pressure indicator persistently illuminates inappropriately 1 Check to ensure all connections are properly and securely connected per instal
2. 5 CLINICAL CARE 160000 Not made with natural rubber latex CLINICAL PLUS ALTERNATING PRESSURE LOW AIR LOSS MATTRESS SYSTEM 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 160000S INS LAB RevC14 CONTENTS HINT PRODUC ON a a a 3 INTENDED USE OF THIS PEVICE 3 CONTRANDICATION 3 IMPORTANT SAFETY PRECAUTIONS sense 4 DANGER vncscsscsssssssssscssssssssscsssssscssssssssscsssssscssssssessessseesessnssstessssnesasssnssaeenessses 4 WARNING 5 NO eeeeetreee eta neta 6 EQUIPMENT SYMBOLS 7 PRODUCT PESCRIPTION 8 PUMP AND MATTRESS SYSTEM 8 PUMP FRONT 8 PUMP REAR 8 PUMP FRONT PANEP 9 FRONT PANEL FIRST ROW CYCLE TIME ADJUSTMENT 9 FRONT PANEL SECOND ROW PRESSURE ADJUSTMENT 9 FRONT PANEL THIRD ROW THERAPY MODE ADJUSTMENT 9 FRONT PANEL FOURTH ROW cssssssssssssssssssssssssssssstsssssesssessasssessaee 10 INSTALLATION Qu ccssssssssssssssscssssssesscssssssesstssssssessnsssesscssaesssssnsssessnssnessessnssaesanseaee 11 UNPACKINGE a nn 11 PUMP AND MATTRESS INSTALLATION rennes 11 OPERATION necssssssssssssssssssscsssssssssssssssscssessssssessesstssessessessnsssessessssaessnssneenesaceses 13 PRESSURE ADJUSTMENT sense 14 QUICK DISCONNECT 14 TRANSPORT CAP 14 CPR FUNC TION re es 15 MAINTENAMN C
3. 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 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 custom
4. E 16 CEANING 16 GENERAL MAINTENANCE 16 FUSE REPLACEMENT nee 17 AIR FILTER REPIACEMENT 17 Cupo eT e Aeon vu A 18 SPECIFICATIONS 19 ONE 1 YEAR LIMITED WARRANTY seems 20 APPENDIX A EMC INFORMATION sense 21 SIMMONS Clinical Care products manufactured by GF Health Products 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 2014 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 760000S INS LAB RevC14 INTRODUCTION Use this manual for set up and operation of the SIMMONS Clinical Care 760000S Clinical Plus Alternating Pressure Low Air Loss Mattress System 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 760000S Clinical Plus Alternating Pressure Low Air Loss Mattress System is e The treatment of pressure ulcers while optimizing user comfort e Pain management as prescribe
5. NT pa WA ick connector PUMP REAR switch power cord receptacle filter 8 760000S INS LAB RevC14 PUMP FRONT PANEL cycle time adjust button cycle time decrease pressure button indicators at right of button pressure level indicators at right of button increase pressure button therapy adjust button therapy mode indicators at right of button panel lock button panel lock indicator at right of button alarm mute button m Obs Prassure a Service e Jer service indicator low pressure indicator upper power ON OFF button ON OFF power failure indicator lower indicator at right of button Front panel first row cycle time adjustment There are four cycle time settings Press the cycle time adjust button to cycle between the settings The selected cycle time setting s indicator will illuminate Front panel second row pressure adjustment There are ten pressure firmness settings Press the decrease pressure button at the left end of the row to decrease pressure softer and press the increase pressure button at the right end of the row to increase pressure firmer The selected pressure level setting s indicator will illuminate Front panel third row thera mode adjustment There are four therapy mode settings Autofirm to fill mattress quickly or to fully inflate mattress during patient ingress egress for better support Alternating Pressure
6. 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 REPAIR 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
7. TICE 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 if it s in alternating mode 4 Check the air hoses for any kink or break For replacement please contact your Graham Field authorized distributor 16 760000S INS LAB RevC14 Fuse replacement l tool needed small screwdriver If you suspect a blown fuse disconnect the plug from the wall outlet immediately Use a small screwdriver to remove 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 l tool needed small screwdriver Use a small screwdriver to remove the air filter plate located at rear of pump filter location is shown in picture at right Remove the filter The filter is reusable if not torn and can be washed gently with a mild detergent and water Dry the filter before use filter Replace the filter and cover Ensure that filter cover is securely installed Replace the air filter regularly if it is gra
8. d 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 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 760000S 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 the Alternating Pressure Low Air Loss 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 usef
9. er 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 W 4 19 1P A 124P D 02 ore CE PE e SOS 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 760000S INS LAB RevC14 23 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
10. g two notches firmer Wait ten minutes and then check again You should only have to adjust this setting one time per patient Please consult your physician for an appropriate setting QUICK DISCONNECT Pull the power plug from the wall connector to disconnect the device quickly TRANSPORT CAP In case of power failure or transport Disconnect the quick connector and cap the mattress with the transport cap to slow deflation a connector ansport cap 14 760000S INS LAB RevC14 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 1 2 Disconnect the quick connector from the pump in the location of the arrow shown at right 760000S INS LAB RevC14 15 MAINTENANCE CLEANING Perform the following cleaning procedures before use 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 bleach diluted in water Air dry all parts thoroughly before use A NOTICE Do not use phenolic products to clean the mattress A NO
11. hould make sure it is used in such an environment IEC60601 Test Level Electromagnetic Compliance z p Environment Guidance Immunity Test Portable and mobile RF communications equipment 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 Recommended separation IEC 61000 4 6 80 MHZ outside distance ISM bands d 1 2 VP 150kHz to 80MHz Radiated RF 3 V m 80 MHz to 3V m IEC 61000 4 3 d 12VP 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 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 760000S INS LAB RevC14 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
12. lated During Autofirm you can preset the device by pressing the Therapy Comfort and Cycle Time buttons and selecting the desired settings The selected indicators will illuminate during Autofirm and the system will automatically operate your settings immediately after the Autofirm process is complete When the selected pressure level is reached the low pressure indicator yellow LED and the Autofirm indicator will de illuminate and the pump will enter alternating mode If not preset as described in step 4 the mattress can now be adjusted to the desired pressure Replace all sheets blankets and pillows on the bed 760000S INS LAB RevC14 13 PRESSURE ADJUSTMENT Generally a lighter patient will need a lower softer setting while a heavier patient will need a higher firmer setting but pressure adjustment must ultimately be based on the patient s weight distribution A short stocky person may be the same weight as a tall thin person but their settings will not be the same The mattress should be firm enough to support the patient yet soft enough so the patient will sink down to eliminate pressure points Initially inflate the mattress to maximum pressure Then when the patient lies on the mattress test the pressure by placing four fingers below the mattress under the patient s buttock area your fingers should just fit If the fit is too loose decrease the setting If your fingers do not fit well increase the settin
13. lation 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 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 indicator Mechanical failure service required contact your Graham Field authorized distributor 10 760000S INS LAB RevC14 INSTALLATION UNPACKING l Before unpacking check for obvious damage to the carton or its contents If damage is evident please notify the carrier and your Graham Field authorized distributor Remove all loose packing from the carton Carefully remove all components from the carton Inspect all components If damage is evident please notify the carrier and your Graham Field authorized distributor PUMP AND MATTRESS INSTALLATION l Place the mattress on top of the bed frame ensure the foot end symbol faces up at foot end as shown at right Secure mattress to bed with straps AAN Fold open the wire hangers on the back of the pump as shown at right 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 NOTICE Place the device in a position where the ca
14. ls 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 purpose 6 760000S INS LAB RevC14 EQUIPMENT SYMBOLS Attention Consult accompanying documents this manual 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 0 Class Il for UL only 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 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 oe with respect to electrical shock fire and 53DG mechanical hazards only in accordance with UL60601 1 and CAN CSA C22 2 No 601 1 760000S INS LAB RevC14 7 PRODUCT DESCRIPTION PUMP AND MATTRESS SYSTEM foot end N lt a gi Le mattress pump connectors f valves mattress pump and mattress system PUMP FRO
15. nd GF shall not be liable for the following 1 Defects damage or other conditions caused in whole or in part by misuse abuse negligence alteration 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
16. od commercial practice and applicable GF instructions and manuals including proper use and maintenance To the extent that a component 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 760000S Clinical Plus Alternating Pressure Low Air Loss Mattress System cccccccsssssssseeeeeeeees 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 a
17. ommercial or hospital IEC61000 4 4 1kV for input out line 1kV for input out line environment 1kV for differential 1kV 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 lt 5 UT gt 95 dip in lt 5 UT gt 95 dip in Mains power quality should be that short UT for 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 UT 30 dip in 70 UT 30 dip injduring power mains interruptions it power supply UT for 25 cycles UT for 25 cycles is recommended that the device be input lines lt 5 UT gt 95 dip in lt 5 UT gt 95 dip in oowered 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 760000S INS LAB RevC14 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 s
18. r particles A WARNING Never drop or insert any object into any opening or hose A A WARNING Connect this product only to a properly grounded power outlet Z WARNING Maximum patient weight capacity for this product is 400 Ib 189 kg EVENLY DISTRIBUTED WARNING 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 760000S INS LAB RevC14 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 rai
19. regiver and or doctor can access it easily Connect the mattress pump air hose quick connector ensure the connector has clicked securely into place before continuing 760000S INS LAB RevC14 11 A NOTICE Ensure that 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 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 12 760000S INS LAB RevC14 Turn the main power switch Press the front panel power OPERATION to the ON position main 4 power switch ri button The power indicator will illuminate ower button Info The mattress system will automatically enter Autofirm mode for the quickest inflation at set up initial inflation takes approximately twenty minutes 3 The pump will begin delivering air into the mattress The low pressure indicator yellow LED and the Autofirm indicator will illuminate until the mattress is fully inf
20. the invoice date GF Health Products Inc 2935 Northeast Parkway Atlanta GA 30360 Tel 770 368 4700 Fax 770 368 2386 www grahamfield com 20 760000S 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 Harmonic emissions 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 En ro Ae Cadance Floors should be wood concrete or Electrostatic ae 6kV contact 6kV contact ceramic tile If floors are covered Discharge ESD 8kV air 8kV air with synthetic material the relative IEC61000 4 2 humidity should be at least 30 Electrical fast 2kV for power supply 2kV for power supply Mains power quality should be that transient burst line line of atypical c
21. ul 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 Z DANGER Do not use this product while bathing Z DANGER Do not place or store 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 Z DANGER Do not reach for a product that has fallen into water Unplug it immediately 4 760000S 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 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 authorized distributor 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 simila
22. y torn or the environment is dirty 760000S INS LAB RevC14 17 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 760000S INS LAB RevC14 SPECIFICATIONS Pump Specification Info see rating label on product Weight ebeo 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 Il 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 C iB 78 7 x 35 4 x 8 200 x 90 x 20 3 cm Weight S BITS HG 760000S INS LAB RevC14 19 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 go

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