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Summary of Contents for Apollo Healthcare Technologies Limited Apollo 5 Plus APHos2
- Page 1 //oHealthcare Technologies ™ Apollo 5 Plus APHos2 ™ Apollo S APHos3 USER MANUAL AHSM-001_Version_5 _08.4.2021 www.apollo-ht.co.uk...
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Page 2: Table Of Contents
TABLE OF CONTENTS PAGE ................2 INSTRUCTIONS ................4 INTRODUCTION .............. 5 PRODUCT DESCRIPTION ................7 INSTALLATION ..................8 OPERATION CLEANING ..................STORAGE ..................................9 MAINTENANCE ................11 SPECIFICATIONS THESE ............. 17 SAVE INSTRUCTIONS... -
Page 3: Instructions
INSTRUCTIONS DANGER -To reduce the risk of electrocution: 1. Do not place or drop into water or liquid. 2. Do not reach for a product that has fallen into water. 3. Do not place or store the product where it may fall into water. 4. - Page 4 SYMBOLS Caution Manufacturer Complies with standards protecting against electric shock for type BF equipment. Consult operating instructions for use Protected against solid foreign objects of 12.5 mm and greater; Protection IP21 against vertically falling water drops Class II Temperature limitation/temperature range Dry clean, Any Solvent Except Trichloroethylene Do Not Iron Tumble Dry, Normal, Low Heat...
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Page 5: Introduction
A. INTRODUCTION For initial set up and for reference purpose, this manual should be read carefully. A.1 GENERAL INFORMATION The unit is for prevention or treatment of pressure ulcers. The unit has been tested and successfully approved by the following regulation: IEC/EN 60601-1 IEC/EN 60601-1-2 IEC/EN 60601-1-11... -
Page 6: Product Description
B. PRODUCT DESCRIPTION 8.1 AIR PUMP AND MATERIALS OOPR Punpurnt ttress System Olli C!llYreC' 8.2 PUMP AND MATERIALS Comfort Adjust button (30 200kg) Power On/Off button Mode button (Alternating/Static) Alarm Mute button Panel Unlock button Fuse AirFilter Mounting Brackets Power Cable Plug... - Page 7 B. 3 FRONT PANEL 1. Comfort (weight) setting indication lights. Adjust the comfort button through the weight settings from 30KG to 200KG, according to the patient's weight. The weight settings should only be used as a comfort setting and as a guide in conjunction with a qualified Clinicians advice for each individual user.
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Page 8: Installation
C. INSTALLATION After delivery check the system for any damage which may have occurred during transit. If damaged in any way contact your supplier immediately. C1 PUMP AND MATTRESS INSTALLATION 1. Place air mattress on top of the bed frame/platform. Please ensure foot sign is at the bottom of the bed. -
Page 9: Operation
D. OPERATION & NOTE: Always read the manual before use. D.1 GENERAL OPERATION 1. Insert the supplied power cable into the side of the pump and the plug into a suitable power supply and press the power on button. 2. Wait for 20-30 minutes (depending on the mattress) for the mattress to be fully inflated by the pump. - Page 10 D.3 PRESSURE SET UP Press the comf ort button to cycle through the dif ferent weight settings until the green LED on the desired weight is illuminated. The alternating or static LED will flash until the pressure in the mattress reaches the desired setting.
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Page 11: Cleaning
E. CLEANING Ensure the system is thoroughly cleaned between Patient use. Wipe the air pump with a damp cloth pre-soaked with a mild detergent and keep it dust free. CAUTION, do soak the pump. Wipe the mattress with a damp cloth pre-soaked with warm water (not to exceed C) containing a mild detergent. - Page 12 G.2 FUSE REPLACEMENT 1. Firstly unplug the pump from the mains. 2. Remove the cover of the fuse with a cross head screwdriver. 3. Insert a new fuse of the correct rating and replace the cover. The fuse should be rated as T1A/250V and CE approved. G.3 AIR FILTER REPLACEMENT 1.
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Page 13: Specifications
H. SPECIFICATIONS An pump Specification AC 120V 50/60 0.1A Power Supply C 230V 50/60 0.06 11W 2.38 gs Operation:10• C o 40• C (50" F to 104" F) so· c Storage: -15" (5" F o 122· in :-15"Clo70"C 5"F o158"F ·ronment Operation: 10% o 90% non-conde sing... - Page 14 10. Technical Specification: Item Specification Power Supply (Note: Seerating label on the product) AC 220-240V 50 Hz, 0.09A (for 230V system) 500mA, 250V Fuse Rating Cycle time 12mins Dimension (L x W x H) 27.5x13.5x9cm Weight 1.3Kg AtmosphericPressure 80KPa to 106KPa Operation: 5°C to 35°C (41°F to 95°F) Temperature Storage: -15°C to 50°C (5°F to 122°F)
- Page 15 Appendix A: EMC Information Guidance and manufacturer’s declaration‐electromagnetic emissions The device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that they are used in such an environment. Emissions test Compliance Electromagnetic environment ‐ guidance RF emissions Group 1 The models device use RF energy only for their internal function. Therefore, their RF CISPR 11 emissions are very low and are not likely to cause any interference in nearby electronic equipment. RF emissions Class B The model P08E are suitable for used in domestic stablishment and in establishment CISPR11 directly connected to a low voltage power supply network which supplies buildings used for domestic purposes. Harmonic Class A emissions lEC 61000‐3‐2 Voltage Complies fluctuations / flicker emissions lEC 61000‐3‐3 Warning: 1. The device should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, the device should be observed to verify normal operation in the configuration in which it will be used. 2. Use of accessories, transducers and cables other than those specified or provided by the manufacturer of this equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this equipment and result in improper operation.
- Page 16 Guidance and Declaration‐electromagnetic immunity The models device intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that they are used in such an environment. Immunity test IEC 60601 Compliance Electromagnetic environment ‐guidance test level level Electrostatic ±8 kV contact ±8 kV contact Floors should be wood, concrete orceramic tile. If discharge ±2 kV, ±4 kV, ±8 kV, ±2 kV, ±4 kV, ±8kV, ±15 kV floors are coveredwith synthetic material, the (ESD) lEC ±15 kV air air relativehumidity should be at least 30 %. 61000‐4‐2 Electrical fast ±2kV for power supplylines ±2kV for powersupply lines Mains power quality should be thatof a typical transient/burs ±1 kV for Input/outputlines commercial or hospitalenvironment. t IEC 61000‐4‐4 Voltage dips, <5 % UT <5 % UT Mains power quality should be thatof a typical short (>95% dip in UT.) (>95% dip in UT.) commercial or hospitalenvironment. If the user of interruptions for 0.5 cycle ...
- Page 17 Recommended separation distances between portable and mobile RF communications equipment and the model P08E The model P08E is intended for use in electromagnetic environment in which radiated RF disturbances is controlled. The customer or the user of the model P08E can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the model P08E is recommended below, according to the maximum output power of the communications equipment. Rated maximum Separation distance according to frequency of transmitter outputPowerof m transmitter W 150kHz to 80MHz to 800MHz to 2,5GHz 80MHz 800MHz d=2.3xP d=1.2xP d=1.2xP 0.01 0.12 0.12 0.23 0.1 0.38 0.38 0.73 1 1.2 1.2 2.3 10 3.8 3.8 7.3 100 12 12 23 For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) ...
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Page 18: Save These Instructions
SAVE THESE INSTRUCTIONS It is recommended to repair or replace the unit, unless this is by qualified personal. To reduce the risk of shock or electrocution do not change or modify the cord or plug in any way. //oHealthcare Technologies For further technical support please visit www.apollo-ht.co.uk... - Page 19 //oHealthcare Technologies Apollo Healthcare Technologies Limited Holme Street, Liversedge, West Yorkshire WF15 6JF Tel: +44 (0) 1924 614567 Fax: +44 (0) 1924 607480 Email: sales@apollo-ht.co.uk www.apollo-ht.co.uk Due to ongoing research and development, Apollo Healthcare Technologies Ltd, reserve the right to change specifications without prior notice. This will not affect the efficacy of the system.
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