Low Air Loss Analog
Contents
1. IEC61000 4 11 lt 5 gt 95 90 dip lt 5 gt 95 dip 5 sec in for 5 sec Power frequency Power frequency magnetic fields should be at levels characteristic of 9 6082 magnete ferd a typical 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 11 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 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 2 P 150kHz to 80MHz d 1 2VP 150kHz to 80MHz d 2 34 P 80 MHz to 2 56 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 b 3Vrms150 kHz to 80 distance in meters m Conducted RF MHz outside ISM bands Field strengths from fixed RF transmitters as determined by an electromagnetic site survey f should be less than the compliance level in each frequen2. 90 non condensing Humidity Storage 10 to 90 non condensing Shipping 10 to 90 non condensing Class II Type BF Applied Part Air Mattress Not suitable for use in the presence of a flammable anesthetic mixture No AP or APG protection Mattress Specification Classification Model 5 Overlay 8 Replacement 200 x 90 x 12 7 cm 200 x 90 x 20 3 cm or 78 7 x 35 4 x 8 Weight 5 2 kg or 11 4 lb 7 5 kg 16 5 Ib Soft to Firm setting A NOTE 1 Consult your Medline representative for further technical documents 2 These specifications are also applicable for other regions operating with the same power supply 3 Mattress dimensions and weight is measured without foam 4 The manufacturer reserves the right to modify the specifications without notice Dimension L x W x H 10 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 Decl
3. electric shock for type BF equipment Attention you should read the accompanying information carefully Attention Observe 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 oe bat 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 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 0197 IEC61000 3 2 IEC 61000 3 3 AN FOR US AND CANADA ONLY lie Certified for Medical Equipment Air Pump with respect to electrical E228589 shock fire and mechanical hazards only in accordance with 5506 US 60601 1 CAN CSA 22 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 h
4. from the bottom gt J and turn the hangers outward or inward to secure f the pump against the railing 1 If no bed railing is available place the pump a flat sturdy surface or the floor beneath the bed 3 Connect the Quick Connector on the air hose from air mattress to the pump unit Quick Connector Slot When you hear a click the connection will be secured N AN NOTE Check and ensure the air hoses are not kinked or tucked under the mattress A A A Plug the power into an electrical outlet with the appropriate voltage NOTE The pump unit must be suitable for the local power voltage NOTE S assure que la pompe est compatible au voltage local ou disponible 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 inflate The low pressure indicator yellow LED will illuminate while the mattress is pressurizing 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 NOTE You can unplug the unit to power off the device NOTE L appareil est galement muni d une fiehe de connexion lectricit CAUTION The pump supplied with the mattress can only be used for the mattresses recommended by
5. pressure ulcers With Static Pressure mode all of the air cells are equally inflated 4 2 Emergency CPR Operations CPR must be performed 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 phenol based products for cleaning A CAUTION Do no dry the mattress in direct sunlight The carrying bag if available should be turned inside out and compl
6. the manufacturer Do not use it for any other purpose applied part air mattress AVERTISSEMENT La pompe ne peut tre utilis e qu avec le matelas design recommand par le manufactureier Ne pas server d ysage autre que celui auquel elle a t con u 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 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 A NOTE Always read the operating instructions before use 4 1 PANEL OPERATIONS 1 2 3 3 J NN NORMAL PRESSURE Low PRESSURE 2 4 ALTERNATE STATIC Pressure Adjustment Knob 4 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 if the pressure is suitable for the patient by sliding hand beneath the air cells at the
7. MEDLINE Alternating Pressure Therapy Pump Overlay Replacement Mattress System SUPRA APL Operating Manual Model No MDT24SUPRAAPL PLEASE READ ALL INSTRUCTIONS BEFORE USE CONTENTS IMFORTANT SAFEGUARDS aires genre acl eer other ta E 2 STINET Wy CHON a 3 2 PRODUC T DESCRIPTION ten aan eaten aes 4 TANS Tee TS Naat es 5 Ae OPERATIONS 7 5 LSE AINIIIN Gos ato aaa Saale ce saat Sa aa cites eee aeecate ead eee a 8 Oe MAT TRESS sete cas anced ons bets 9 ee NANG Biased E 9 9 TEGANICAC DESCRIP TON 10 APPENDIX A EMG INFORMATION ais ee da anes 11 IMPORTANT SAFEGUARDS READ ALL INSTRUCTIONS BEFORE USE DANGER To reduce the risk of electrical shock 1 Always unplug this product immediately after using 2 Do not use while bathing 3 Do not place or store product where it can fall or be pulled into a tub or sink 4 Do not place in or drop into water or other liquids 5 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 This product should never be left unatten
8. aration 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 immunity 193 test level Compliance Environment Guidance Floors should be wood concrete or Electrostatic Discharge ESD 6kV contact 6kV contact ceramic tile If floors are covered 1 61000 4 2 8kV air 8kV air with synthetic material the relative humidity should be at least 30 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 line s to Mains power quality should be that line s line s of a typical commercial or hospital 2 kV line s to earth environment Surge IEC61000 4 5 lt 5 Ur gt 95 dip lt 5 Ur gt 95 dip Mains power quality should be that in 0 5 cycle in for 0 5 cycle of a typical commercial or hospital perona a Wea variations on power supply quires continued operation input lines 70 95 Ux 30 dip 70 30 dip in during power mains interruptions it U for 25 cycles for 25 cycles is recommended that the device be powered from an uninterruptible power supply or a battery Voltage dips short
9. cy Radiated RF range 3 V m 80 MHz to 2 5 IEC 61000 4 3 GHz IEC 61000 4 6 Interference may occur in the vicinity of equipment marked with the following 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 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 12 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 use
10. d 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 output power of transmitter 150 kHz to 80 MHz 80 MHz to 800 2 800 MHz to 2 5 GHz d 1 2 4P Separation distance according to frequency of transmitter m 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 n
11. ded when plugged in Close supervision is necessary when this product is used by on or near children or 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 7 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 8 Never drop or insert any object into any opening or hose on this product 9 Connect this product to a properly grounded outlet only See Grounding Instructions O A O NOTEs CAUTIONs AND WARNINGs NOTE Calls attention to useful information tips and 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 m Authorized representative in the European community Manufacturer Complies with standards protecting against
12. elp and reduce the incidence of pressure ulcers while optimizing patient comfort For long term home care of patients suffering from pressure ulcers 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 A NOTE L quipement ne peut tre utilis s il a risque de m lange d un anesth sique inflammable avec l air ou ou oxyde nitreux 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 1 Power Switch 3 2 Power Cord 2 2 3 Bed Frame Hangers 2 I 3 Rear View J 3 INSTALLATION Unpack the box and check the package contents for completeness Package Content List Mattress unit x 1 may not be included if only pump unit is purchased Pump Unit x 1 m User Manual x 1 Inspect equipment for damage which may have occurred during shipment If there is damage please contact your dealer immediately 3 1 PUMP amp MATTRESS INSTALLATION 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 2 Place the pump hangers over the bed railing at the J foot of the bed Support the pump
13. etely 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 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 A 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 excess 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 onthe 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 8 TECHNICAL DESCRIPTION Specifications Item Specification Power Supply Note See AC 120V 60 Hz 0 16 A 14W For 120V System rating label on the product 230V 50 Hz 0 06 12W For 230V System Fuse Rating Dimension RN x W xH 29 x 18 5 x 12 6 cm or 11 4 x 7 3 x 5 0 Weight oo ht 2 2 Kg or 5 Ib Operation 10 to 40 C 50 F to 104 F Temperature Storage 15 C to 50 C 5 F to 122 F Shipping 15 to 70 C 5 F to 158 F Environment Operation 10 to
14. 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 A 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 inflated avoiding prolonged pressure on any single point beneath the patient this is to prevent
15. ot apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people MEDLINE INDUSTRIES INC One Medline Place Mundelein IL60060 4486 TEL 800 MEDLINE 13
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