Product Manual - Drive Medical
Contents
1. 6kV contact 6kV contact TEC61000 4 2 8kV air 8kV air 2kV for power 2kV for power Electrical fast transient burst supply line supply line IEC61000 4 4 1kV for input out 1kV for input out line line Mains power quality should be that of a typical commercial or hospital environment 1 kV line s to 1 kV lines to Mains power quality should be that line s line s of a typical commercial or hospital IEC61000 4 5 2 kV line s to earth 2 kV line s to earth environment Surge lt 5 Uz gt 95 dip lt 5 U gt 95 dip Mains power quality should be that in U for 0 5 cycle in U for 0 5 cycle enue of a typical commercial or hospital Voltage dips short ae MENS m 40 U 60 dip in 40 U 60 dip in environment If the user of this interruptions and voltage variations on power supply U for 5 cycles Ur for 5 cycles device requires continued operation input lines 70 U 30 dip in 70 U 30 dip in during power mains interruptions it U for 25 cycles U for 25 cycles is recommended that the device be IEC61000 4 11 powered from an uninterruptible lt 5 Ur gt 95 dip lt 5 U gt 95 dip power supply or a battery in U for 5 sec in Uy for 5 sec Power frequency Power frequency magnetic fields should be at levels characteristic of eon Magnetic meia a typical location in a typical IEC61000 4 8 commercial or hospital environment NOTE U is the a c mains voltage2. prior to the application of the test level 12 SAVE THESE INSTRUCTIONS GROUNDING INSTRUCTIONS This product should be grounded In the event of an electrical short circuit grounding reduces the risk of electric shock by providing an escape wire for the electric current This product is equipped with a cord having a grounding wire with a grounding plug The plug must be plugged into an outlet that is properly installed and grounded DANGER Improper use of the grounding plug can result in a risk of electric shock If repair or replacement of the cord or plug is necessary do not connect the grounding wire to either flat blade terminal The wire with insulation having an outer surface that is green with or without yellow stripes is the grounding wire NOTE If the repair or replacement of the cord is necessary please contact a qualified electrician or serviceman To reduce the risk of electric shock do not modify the cord or plug in any way Check with a qualified electrician or serviceman if the grounding instructions are not completely understood or if in doubt as to whether the product is properly grounded 11 2 PRODUCT DESCRIPTION 2 1 PUMP AND MATTRESS SYSTEM 1 CPR Tags 2 Pump unit 3 Mattress unit 4 Quick Connector 2 2 PUMP UNIT Front View 1 Quick Connector Slot 2 Front Panel 3 Rear View 1 Power Switch 4 2 Power Cord 3 Mounting Brackets 4 Air Filters 3 INSTALLATION Unpack the
3. box and check the package contents for completeness 8 TECHNICAL DESCRIPTION Specifications Package Content List m Mattress unit x 1 may not be included if only pump unit is purchased Item Specification E Pump Unit x 1 Power Supply Note See AC 100 120V 60 Hz 0 16 A 14W For 120V System m User Manual x 1 rating label on the product Inspect equipment for damage which may have occurred during shipment If there is damage please Fuse Ranny contact your dealer immediately Cycle time Fixed 8 min 60Hz Dimension L x W x H 29 x 18 5 x 12 6 cm or 11 4 x 7 3 x 5 0 3 1 PUMP amp MATTRESS INSTALLATION Weight 2 2 Kg or 5 Ib Operation 10 C to 40 C 50 F to 104 F Temperature Storage 15 C to 50 C 5 F to 122 F Shipping 15 C to 70 C 5 F to 158 F Environment i Operation 10 to 90 non condensing 1 Place the mattress or pad on top of a bed frame Orient the mattress so that the foot markers on the mattress are situated towards the end of the bed where pump will be located Humidity Storage 10 to 90 non condensing Shipping 10 to 90 non condensing Class II with functional earth NOTE 5 Type BF IPX0O Applied Part Air Mattress Classification Not suitable for use in the presence of a flammable Ay anesthetic mixture No AP or APG protection J ka Mattress Specification 2 Place the pump hangers over the bed railing at the 8 Replacement foot of the bed Support the pump from t
4. cally with accuracy To assess the electromagnetic environment due to fixed RF transmitters an electromagnetic site survey 4 O P E R ATION S 7 should be considered If the measured field strength in the location in which the device is used exceeds the E R E E E A A A EA E A G E E E N 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 SSG EP ANIN G eera estes teeadierieestenrieestee temic eieete weenie ee stenes 8 d Over the frequency range 150 kHz to 80 MHz field strengths should be less than 3 V m AI IIR ONAN OIE idi EEE 9 7 MAINTENANCE wcseice cts ctcaucce cies aioeedesateecieaseaciesaieaiesateacienaseaeds 9 a l Recommended separation distances between portable and mobile RF 8 TECHNICAL DESCRIPTION 10 communications equipment and this device This device is intended for use in an electromagnetic environment in which radiated RF disturbances are APPEN D IX A EM C IN F ORM ATI ON D controlled The customer or the user of this device can help prevent electromagnetic interference by Ne ee eee N AA MA one A A aa Ma aaaea aaa Maea ATES BeAr Mia manida aaa Ble eoar RIT maa mia E 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
5. drive Drive Medical Design amp Manufacturing 99 Seaview Boulevard Port Washington NY 11050 Toll Free 877 224 0946 Local 516 998 4600 www drivemedical com REV3 8 29 14 746002 5150 V1 0 1 Air AS5000 AS5000 RR AS5300 Low air loss Alternating pressure mattress Instruction Manual PLEASE READ ALL INSTRUCTIONS BEFORE USE CO NTE NTS 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 IMPORTANT SAFEGUARDS vivsvssereeeeasnrseivaiavsvtealdveeareeesviaaests 2 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 1 INT ROD UCTION etree ttre tere errr eee eee eee eee eee rere eee rer 3 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 2 PRODUCT DESCRIPTION crura corsiieddvncdcedsietleedslieds 4 c Field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land 3 i INSTALL AT ON aaa cs ated a A I A a tt Bhan a a 5 mobile radios amateur radio AM and FM radio broadcast and TV broadcast cannot be predicted theoreti
6. e proper Disposal of Electrical amp Electronic Equipment WEEE This product should be handed over to an appropriate collection point for the recycling of electrical and electronic equipment For more detailed information about the recycling of this product please contact your local city office household waste disposal service or the retail store where you purchased this product Consult operating instructions Class Il Functional earth 1 INTRODUCTION This manual should be used for initial set up of the system and for reference purposes 1 1 GENERAL INFORMATION This system is a high quality affordable mattress system suitable for the treatment and prevention of pressure ulcers This product has been tested and successfully approved for the following standards EN 60601 1 EN 60601 1 2 EN 55011 Class B IEC61000 3 2 IEC 61000 3 3 AN FOR US AND CANADA ONLY PSSIF Medical Equipment Air Pump E465930 d with respect to electrical shock fire and 53DG C US mechanical hazards only in accordance with UL60601 1 AND CAN CSA C22 2 NO 601 1 Le produit a t test avec des quipements m dicaux et respecte les normes UL 60601 1 amp CAN CSA C22 2 No 601 1 pr venant les choc lectrique le feu et les risques de blessures physiques 1 2 INTENDED USE This product is intended E to help and reduce the incidence of pressure ulcers while optimizing patient comfort m for long term home care of patients suffering fr
7. equipment Rated maximum output power of transmitter 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz d 1 24P Separation distance according to frequency of transmitter m For transmitters rated at a maximum output power not listed above the recommended separation distance a 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 Guidance and Manufacturer s Declaration Electromagnetic mmunity 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 I EC60601 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 2 P 150kHz to 80MHz d 1 2J P 150kHz to 80MHz d 2 3 P 80 MHz to 2 5G MHz Where P is the maximum
8. he bottom l Z J 200 x 90 x 20 3 cm and turn the hangers outward or inward to secure Dimension L x W x H the pump against the railing We or 78 7 x 35 4 x 8 If iling is avai f ii Weight 7 5 kg 16 5 Ib no bed railing is available place the pump on a flat i Pressure Range Adjustable Weight Settings Weight Settings sturdy surface or on the floor beneath the bed bei l A NOTE 1 Consult the distributor or EU representative for further technical documents 2 These specifications are also applicable for other regions operating with the 3 Connect the Quick Connector on the air hose from same power supply air mattress to the pump unit Quick Connector Slot When you hear a click the connection will be secured 3 The manufacturer reserves the right to modify the specifications without notice e 4 The earthing terminal is served as functional earth not protective earth not kinked or tucked under the S A NOTE Check and ensure the air hoses are i mattress 5 10 6 MATTRESS STORAGE 1 Lay the mattress on a flat surface upside down 2 Roll up the mattress starting from the head until you reach the foot of the mattress 3 Use the straps at the end of the mattress and stretch them around the mattress to prevent it from unraveling AN Note Do not fold crease or stack the mattresses 7 MAINTENANCE 7 1 GENERAL 1 Check the main power cord and plug for abrasions or e
9. ice NOTE L appareil est galement muni d une fiehe de connexion a l lectricit A CAUTION The pump supplied with the mattress can only be used for mattresses recommended by the manufacturer Do not use it for any other purpose applied part air mattress AN AVERTISSEMENT La pompe ne peut tre utilis e qu avec le matelas designe ou r recommand par le manufactureier Ne pas server d ysage autre que celui auquel elle a t con u A NOTE For models WITHOUT the low air loss function During power outages you can cover the Quick Connector with the transport cap to maintain air pressure inside the air cells A NOTE After installation make sure any excess cord or tubing is removed from possible foot traffic to avoid accidental tripping All EQUIPMENT should be positioned to always allow unhindered patient access by physicians and caregivers 4 OPERATIONS AN NOTE Always read the operating instructions before use 4 1 PANEL OPERATIONS 1 Pressure Adjustment Knob The pressure adjustment knob controls the air pressure in the mattress Turning the knob clockwise will increase the pressure counter clockwise decreases the pressure Higher pressures will support heavier patients The pressure should be adjusted according to individual comfort preferences When the mattress is finished pressurizing to the desired level of firmness the Normal Pressure LED indicator will illuminate NOTE You can also check
10. if the pressure is suitable for the patient by sliding one hand beneath the air cells at the level of the patient s buttocks The air cells will alternately inflate and deflate You should feel slight contact with the buttocks when the air cells beneath the buttocks deflate A NOTE Every time the mattress is initialized inflated it is recommended that you set the pressure knob to Max to hasten inflation You can then adjust the air mattress to the desired firmness later Normal Pressure Indicator When the green LED illuminates the pressure inside of air mattress has reached the desired pressure setting preset on the Pressure Adjustment Knob Low Pressure Indicator When the mattress is initializing the Low Pressure LED will illuminate until the appropriate pressure is reached according to the Pressure Adjustment Knob this is normal Otherwise the Low Pressure LED is a warning indicating that the pressure in mattress is unusually low Check to ensure all connections are secured and correctly installed as per the installation instructions AN NOTE If the pressure level is consistently low check for any leakage tubes or air hoses If necessary replace any damaged tubes or hoses or contact your local qualified dealer for repair 4 Alternate Static Switch The ALTERNATE STATIC switch selects between Alternate Pressure mode and Static Pressure mode With Alternate Pressure mode alternating air cells are partially deflated and i
11. invalids Use this product only for its intended use as described in this manual Do not use attachments not recommended by the manufacturer Never operate this product if it has a damaged cord or plug if it is not working properly if it has been dropped or damaged or exposed to water Return the product to a service center for examination and repair Keep the cord away from heated surfaces Never block the air openings of this product Never place the product on a soft surface such as a bed or couch where the air openings may become blocked Keep the air openings free of lint hair and other similar particles Never drop or insert any object into any opening or hose on this product Connect this product to a properly grounded outlet only See Grounding Instructions NOTEs CAUTIONs AND WARNINGs NOTE Calls attention to useful information tips reminders CAUTION Calls attention to correct operating or maintenance procedures in order to prevent damage to or destruction of the equipment or other property WARNING Calls attention to a potential danger that requires correct operating procedures or practices in order to prevent personal injury SYMBOL Definitions Hoe Dt PB Authorized representative in the European community Manufacturer Complies with standards protecting against electric shock for type BF equipment Attention you should read the accompanying information carefully Attention Observ
12. nflated avoiding prolonged pressure on any single point beneath the patient this is to prevent pressure ulcers With Static Pressure mode all of the air cells are equally inflated 4 2 Emergency CPR Operations CPR must be performed on a firm surface Therefore if an emergency CPR situation occurs with the patient on the mattress the mattress must be quickly deflated This is done by quickly pulling on the CPR tag located at the head of the mattress on the patient s right side The quick connector found from the pump unit can also be disconnected to hasten deflation 5 CLEANING It is important to follow the cleaning procedures before first time use with any patient this is to avoid the possibility of transmission of pathogens between patients and caregivers Wipe down the pump unit with a damp cloth pre soaked with a mild detergent Avoid contact with dust and proximity to dusty areas Make sure that any cleaning agents you use will not harm or corrode the plastic casing on the pump unit A CAUTION Do not immerse or soak the pump unit in liquids Wipe down the mattress unit with a damp cloth pre soaked with warm water do not exceed 65 C containing a mild detergent Avoid dust and proximity to dusty areas The cover may also be cleaned using sodium hypochlorite diluted in water All components should be air dried thoroughly before use A CAUTION Do not use phenolic based products for cleaning A CAUTION Do no dry the mattre
13. om pressure ulcers E for pain management as prescribed by a physician A NOTE This equipment is not suitable for use in the presence of flammable anesthetic mixture with air or with pure oxygen or nitrous oxide AN NOTE L equipement ne peut tre utilis s il y a risque de m lange d un anesth sique inflammable avec l air ou l oxyg ne ou oxyde nitreux 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 Class A IEC61000 3 2 The device is suitable for use in all establishments including domestic establishments and those directly Voltage fluctuations connected to the public low voltage power supply Flicker emissions Complies network TEC61000 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 Electromagnetic zmmumey rest test level Compliance Environment Guidance Floors should be wood concrete or ceramic tile If floors are covered with synthetic material the relative humidity should be at least 30 Electrostatic Discharge ESD
14. output power rating of the transmitter in watts W according to the transmitter manufacturer and d is the recommended separation f 6 3Vrms150 kHz to 80 distance in meters m Conducted RF MHz outside ISM bands i IEC 61000 4 6 Field arenge from fixed RF TA as determined by an electromagnetic site survey should be less than the compliance level in each frequency d Radiated RF range 3 V m 80 MHz to 2 5 I EC 61000 4 3 GHz Interference may occur in the vicinity of equipment marked with the following symbol a 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 13 IMPORTANT SAFEGUARDS READ ALL INSTRUCTIONS BEFORE USE DANGER To reduce the risk of electrical shock 1 2 3 4 5 Always unplug this product immediately after using Do not use while bathing Do not place or store product where it can fall or be pulled into a tub or sink Do not place in or drop into water or other liquids Do not reach for a product that has fallen into water Unplug immediately WARNING To reduce the risk of burns electrical shock fire or injury O A OON N O 8 9 This product should never be left unattended when plugged in Close supervision is necessary when this product is used by on or near children or
15. ss in direct sunlight The carrying bag if available should be turned inside out and completely wiped down using disinfectant solutions Allow it to air dry thoroughly and then turn it back and wipe down the outside of the bag with disinfectant solutions
16. xcess wear 2 Check the mattress cover for signs of wear or damage 3 Disconnect the air tube from the mattress Then check the airflow coming from the two air outlets on the pump They should be alternately delivering air when the pump is set at alternate mode 4 Check the air hoses for kinks or breaks For replacement please contact your local distributor 7 2 AIR FILTER REPLACEMENT 1 Open the air filter cap located at the back of pump 2 The filter is reuseable and can be washed gently with mild detergent and water Dry the filter before use 3 Check and replace air filter regularly if environment is dirty Air Filter Air Filter Cap 4 Plug the power cord into a electrical outlet with the appropriate voltage f NOTE The pump unit must be suitable for the local power voltage NOTE S assure que la pompe est compatible ft au voltage local ou disponible 6 Turn the main power switch on pump to the ON position After you turn on power to the pump you will have to wait at least 20 minutes for the mattress to become fully inflated 3 D ON The low pressure indicator yellow LED will pa illuminate while the mattress is pressurizing AN When the appropriate pressure is reached the Low Pressure indicator yellow LED will go off and the Normal Pressure indicator green LED will illuminate The bed is now ready for use A NOTE You can unplug the unit to power off the dev
Download Pdf Manuals
Related Search