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 CE Mark Manufacturer Complies with standards protecting against electric shock for type BF equipment. Consult operating instructions for use IP21 Protected against solid foreign objects of 12.5 mm and greater; Protection 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...
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...
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 150kg) Power On/Off button Low Pressure Indicator Normal Pressure Indicator Panel Tactile Fuse AirFilter Mounting Brackets Power Cable Plug...
Page 7
B. 3 FRONT PANEL 1. Comfort (weight) setting adjust dial. Adjust the comfort dial through the weight settings from 30KG to 150KG, 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.
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.
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. Turn the comfort setting to desired level and 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 Turn the comf ort dial to select dif f erent weight settings. Turning clockwise will increase the pressure in the mattress and turning anti-clockwise will decrease the pressure in the mattress. The Low Pressure LED will light until the pressure in the mattress reaches the desired setting and then the Normal Pressure LED will light.
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. Lr:. 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 T1 A/250V and CE approved. G.3 AIR FILTER REPLACEMENT 1.
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...
10. Technical Specification: Item Specification Power Supply (Note: Seerating label on the product) AC 220-240V 50 Hz, 0.09A (for 230V system) Fuse Rating T500mAH, 250V Cycle time 12mins Dimension (L x W x H) 27.5x13.5x9cm Weight 1.3Kg AtmosphericPressure 80KPa to 106KPa Operation: 5°...
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...
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...
Page 17
Recommended separation distances betweenportable and mobile RF communications equipment and the model P08 The model P08 Series is intended for use in electromagnetic environment in which radiated RF disturbances is controlled. The customer or the user of the model P08 Series can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the model P08 Series are recommended below, according to the maximum output power of the communications equipment.
Page 18
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
Tel:Fax: +48 509 778 660 Email: info@pamed-consulting.eu 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. Always consult the user manual for instructions for use.
Need help?
Do you have a question about the 5 Premium and is the answer not in the manual?
Questions and answers