OSKA Dynaform Alternating Air Cushion User Guide

June 16, 2024
Oska

OSKA Dynaform Alternating Air Cushion

Product Information

Specifications

  • Product Name: Dynaform Alternating Air Cushion
  • Version: 1 – 09.08.2023
  • Manufacturer: Apollo Healthcare Technologies Ltd.
  • Manufacturer Address: Unit 1A Gildersome Spur, Morley, Leeds, LS27 7JZ, UK
  • Manufacturer Phone: +44 (0) 1924 614567
  • Manufacturer Fax: +44 (0) 1924 607480
  • Manufacturer Email: info@apollo-ht.co.uk
  • Manufacturer Website: www.apollo-ht.co.uk
  • EC REP: PaMed Consulting Karol Pawelec ul. Jeleniowska 202A/54, 25-564 Kielce, Poland
  • EC REP Phone/Fax: +48 507 833 787
  • EC REP Email: ar@pamed-consulting.eu

Introduction

  • Congratulations on the purchase of your Dynaform Alternating Air Cushion. This cushion is designed to help reduce the incidence of pressure ulcers and optimize patient comfort.
  • It is made of durable, high-quality materials to ensure long-lasting and uninterrupted performance.

Product Features

  • Alternating pressure air pump powered by an internal lithium battery
  • Molded visco foam cushion base with 6 alternating cells
  • Installed on a wheelchair and used as a cushion

Safety Precautions

To use this product safely, please read and understand the following safety precautions:

  • Read and follow the instructions in the user manual carefully.
  • Be aware of potential dangers and follow the defined warnings in the manual.

Confirm before using

  • Check the packing list to ensure all components are included.

User Instructions

Air Pump Output Pressure Check

  1. Ensure the air pump is connected to the cushion.
  2. Turn on the air pump.
  3. Check the output pressure on the air pump display.

Cushion Cleaning

  1. Remove the cushion from the wheelchair.
  2. Wipe the cushion with a damp cloth and mild detergent.
  3. Allow the cushion to air dry before reusing it.

Air Pump Cleaning

  1. Disconnect the air pump from the cushion.
  2. Wipe the air pump with a damp cloth.
  3. Do not immerse the air pump in water.
  4. Allow the air pump to dry before reconnecting it to the cushion.

Storage and Disposal Methods

  • Store the cushion and air pump in a clean and dry place.
  • If discarding the product, send it to an appropriate recycling facility.

Troubleshooting Guide

  • If you encounter any issues with the product, refer to the troubleshooting guide in the user manual for assistance.

Warranty and After-sales Service

  • Please read the warranty and after-sales service information provided in the user manual carefully.

EMC Declaration

  • The product complies with the EMC requirements specified in the user manual.

FAQ

Q: What is the intended use of the Dynaform Alternating Air Cushion?

  • A: The cushion is intended to help reduce pressure ulcers and optimize patient comfort.

Q: How should I clean the cushion?

  • A: Remove the cushion from the wheelchair and wipe it with a damp cloth and mild detergent. Allow it to air dry before reusing.

Q: Can I wash the cushion?

  • A: No, do not wash or bleach the cushion. Wipe it with a damp cloth instead.

Q: How do I check the air pump output pressure?

  • A: Connect the air pump to the cushion, turn it on, and check the output pressure on the air pump display.

Know your symbols

OSKA-Dynaform-Alternating-Air-Cushion-FIG-1

Introduction

  • Congratulations on the purchase of your Dynaform Alternating Air Cushion. The durable, high-quality material used in the manufacturing of these products will ensure that you experience long-lasting and uninterrupted performance.

Intended Use

  • This product is intended to help and reduce the incidence of pressure ulcers while optimizing patient comfort. It also provides the following benefits:
  • To help 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.
  • The product can only be operated by personnel who are qualified to perform general nursing procedures and have received adequate training in knowledge of prevention and treatment of pressure ulcers.

Contraindication

  • Patient conditions for which the application of pressure relieving therapy on an alternating system are contraindicated as follows:
  • Cervical or skeletal traction
  • Unstable spinal cord injuries

Products Features

  1. The product consists of an alternating-pressure air pump powered by an internal lithium battery and a molded visco foam cushion base with 6 alternating cells. It is generally installed on a wheelchair and used as a cushion.

Safety Precautions

  • To use this product safely, please read this IFU carefully and understand it. Please be sure to follow the instructions in this manual.
  • To avoid a disaster when using this product, you must know in advance the factors that may be dangerous. However, it is difficult to predict all potential dangers.
  • Therefore, warnings about security are defined and described in this manual.

WARNING!

  • If you do not follow the instructions in this symbol, you are warned that there is a risk of property damage, injury, or death. Because it is especially important, it is described below as “safety precautions and warnings”

Safety Warnings

  • WARNING! This product features a layer of soft air floating beneath the patient’s body. Therefore, do not use it when patients need to undergo cardiac resuscitation.
  • WARNING! Use this product with your doctor or specialist when using this product. In addition, if the body feels abnormal during use, or the symptoms are worse, or there is a risk of accident, stop using it immediately and consult an expert.
  • WARNING! When you move to a stand position or get out of the cushion, be sure to ask someone else for assistance, otherwise there is a danger of falling.
  • WARNING! Smoking is not allowed on the cushion and may cause a fire.
  • WARNING! Please do not bundle the air outlet or press it under the cushion. When the blower tube is bent or compressed, air may not enter the air mattress and may not achieve the desired results.
  • WARNING! Do not use the air pump in a damp place. Do not use in or around water or urine, which may result in electric shock or malfunction. Avoid direct sunlight.
  • In hot and humid places, keep it away from the wall or above 55cm to avoid moisture retention.
  • WARNING! Please do not remove the screw of the air pump to open the casing and repair it yourself; it may cause electric shock or malfunction.
  • In addition, the modification of the air pump without our consent may pose a serious safety hazard. Never let customers modify the air pump.
  • WARNING! If you do not use the air pump for a long time or need to clean the air pump, be sure to unplug the power cord from the outlet. If not it may cause accidents, electric shocks, and malfunctions.
  • WARNING! Please do not pull on the power cord of the air pump, do not damage the power cord, and do not clip the power cord to the door. When removing the plug from the socket, be sure to hold the power plug and pull it out to avoid electrical accidents and fire.

Confirm before using

  • Before using, please confirm whether the accessories are complete and whether you understand the contents and precautions of the manual.

Packing list confirmation

  1. Air pump for cushion x1
  2. Power cord x1
  3. Power Adapt x1
  4. User manual x1
  5. Cushion x1OSKA-Dynaform-Alternating-Air-Cushion-FIG-3

User instructions

Step 01 Place the cushion on the chair

N.B. Actual cushion may look different to that shown in the image
Step 02:

  • Hang the hooks of the air pump on the chair frame or put on a nearby platform if the chair is not moving
  • Connect the air pipes using the quick connector to the side of the pump
  • N.B. Actual pump may look different from the above image

Step 03

  • Turn On the power
  • Adjust the Pressure
  • Adjust the Function
  1. Power: Press this button to turn the pump on and off.
  2. Pressure: Press this button to cycle through the 3 pressure settings
    • LOW = 20mmHg
    • MEDIUM = 40mmHg
    • HIGH = 60mmHg
  3. Static: Press this button to cycle through the Static & Alternate settings:
    • The default setting is 6 min alternating cycle. You can select to put the pump into a static function for 10 min or 20 min.
    • After the selected time has elapsed, the pump automatically defaults to 6 min alternating cycle
  4. Battery Indicator: This shows the level of charge currently in the battery.
    • When all 4 lights are illuminated green, the battery is fully charged.
    • As power is used, the number of lights illuminated reduces.
    • When there is only 1 light left, it is time to charge the battery.
  5. Charging Indicator: When the power adapter provided with the pump is connected to the pump and a suitable power supply, the charging indicator symbol is illuminated green.
  • As the battery charges the lights on the battery symbol illuminate gradually from no lights to 4 lights and then all lights extinguish and the sequence starts again until the battery is fully charged.
  • When the battery is fully charged, all 4 lights on the battery symbol remain illuminated constantly.
  • Once the battery is fully charged remove the power adapter from the pump, although there is a safety feature to prevent overcharging.
  • Step 04: Terminate the operation of the device
  • When you do not need to use the device, turn off the power to save the charge in the battery.

Battery Charge!

  • Please use the adapter provided by the manufacturer to charge the battery, otherwise, it may cause the battery to affect the life of the battery, cause the battery to overcharge, or cause fire and other hazards.

Maintenance

  • Warning! Do not carry out maintenance when the product is in use.

Air pump output pressure check

  • In the case of air pumps and air cushions, please check the pressure once a week.
  • In addition, if you change the location, or if you suspend operation due to power outages, etc., please do it every time, even within a week.

Cushion cleaning

  • Usually use a dry cloth to clean the cushion
  • If necessary, wet the cloth with a neutral detergent, wring the cloth, and clean the cushion cover.
  • Let it dry naturally
  • Maintenance is required when the product is no longer in use.
  • Maintenance is required when the cushion is contaminated by the patient’s bodily fluids. If the inner foam becomes wet, it must be replaced.
  • Maintenance is required every other week when in use.

Warning!

  • Dry cleaning is forbidden, otherwise, it will hurt the cushion
  • Please do not use a dryer to avoid deformation of the cushion.
  • Do not use an iron to avoid damage to the cushion cover

Air pump cleaning

  • Turn off the power switch and unplug the power cord.
  • Usually use a dry cloth to clean the air pump.

Storage and disposal methods

If you are no longer using this product, please follow the steps below.

  1. Turn off the power switch and unplug the power cord.
  2. Unplug the air tube
  3. Cleaning dirty air pumps and cushions
  4. Do not fold the cushion and put it in the plastic bag
  5. Tighten the power cord and put the air pump in a plastic bag.
  6. Put the air pump and cushion in the box, together with this manual

NOTE:

  • Please put it in a stable place, do not drop from a height.
  • Please do not put heavy objects on the box.
  • Please keep it in a place with low humidity.

Troubleshooting guide

Trouble/Possible Reason

The pump does not start, no light on power button| The battery is flat or the power plug is not plugged into the power outlet,

the power supply does not work.

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The air cushion is too soft| •  Valve does not work

• The connector is off

•  Air pipes kinked

•  Damaged cell inside cushion

The air cushion is too Firm| Pressure Selection error
Air pump noise is abnormally high| •  Put something on the air pump

•  The air pump is in contact with other things

•  Put the air pump on something easy to vibrate

Power outage| •  The power plug

•  Internal fault

Technical Service: 02394 318 318

Warranty and after-sales service (Please read carefully)

Service life and Shelf life

  • THE EXPECTED SERVICE LIFE OF the pump is 5 years
  • THE EXPECTED SERVICE LIFE OF the cushion is 2 years

Warranty

Item/Warranty

  • Pump 24 months
    • Cushion 12 months

About the repair request

  • First, look at the possible causes (see page 14). If you are still having trouble, turn off the product and contact your dealer or Apollo Healthcare Technologies.

During the warranty period

  • In the event of a malfunction in a normal use condition, your dealer should repair it according to the provisions of the warranty.
  • Please show your warranty when you are under warranty.
  • In addition, if the second article of the guarantee is met, the repair is charged. Please confirm the guarantee for details.

After the warranty expires

  • Please consult with the shop or company you purchased, and if you can maintain the function through maintenance, you can repair it at a charge according to the customer’s request

Service personnel requirements

  • Should have a certain understanding of the product.
  • Should be able to understand the circuit schematic.
  • Should be able to use a screwdriver, soldering iron, multimeter, etc.
  • We (the manufacturer) will provide the technical instructions, the circuit diagram, parts list to the service personnel.

Warning!

  • Please don’t replace the power cord by yourself and it must be replaced by professional service personnel.
  • The parts should be replaced by professional service personnel when it is necessary to be replaced.
  • The only safe way to turn off the power completely is to unplug the power cord

Specification list

Specifications

Adapt Power Supply| Input: AC 100-240Vac 50/60Hz 1.6A

Output: 28Vdc 2.0A

---|---
Adapt dimension(LxWxH)| 12×13.5×5.5 cm
Internal Li-Battery| 22.2Vdc 2000mAH
Work time when the battery is fully charged| 8 hours
Cycle time| 6 mins, Fixed, non-adjustable (*Customization)
Dimension(LxWxH)| 27.5x14x9.5 cm
Weight| 1.8Kg
Environment| Atmospheric pressure| 80KPa to 106KPa
Temperature| Operation: 5°C to 40°C (50°F to 104°F) Storage: -15°C to 70°C (5°F to 158°F) Shipping: -15°C to 70°C (5°F to 158°F)
Humidity| Operation: 10% to 90% non-condensing

Storage: 10% to 90% non-condensing

Shipping: 10 % to 90% non-condensing

Classification| Class II, Type BF, IP21

Applied part: Air mattress/Air pad

Not suitable for use in the presence of a flammable

Anesthetic mixture (No AP or APG protection)

Cushion| Size 45x45x10cm Weight:1.0Kg

EMC Declaration

EMC information Guidance and manufacturer’s declaration-electromagnetic emissions

The device is intended for use in the electromagnetic environment specified below.

The customer

Emissions test Compliance Electromagnetic environment – guidance
RF emissions CISPR 11 Group 1 The model’s device uses RF energy only for its

internal function. Therefore, their RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.
RF emissions CISPR11| Class B| The models P01, and P05 are suitable for use in domestic establishments and in establishments directly connected to a low- voltage power supply network that supplies buildings used for domestic purposes.
Harmonic emissions lEC 61000-3-2| Class A
Voltage fluctuations

/ flicker emissions lEC 61000-3-3

| Complies
Warning:

01.  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.

02.  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.

03.  Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the Pump, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result.

Guidance and Declaration-electromagnetic immunity

  • The model P08M device is intended for use in the electromagnetic environment specified below.
  • The customer or the user of the device should ensure that they are used in such an environment.

Immunity test| IEC 60601 test level| Compliance level| Electromagnetic environment -guidance
---|---|---|---
Electrostatic discharge (ESD) lEC 61000-4-2| ±8 kV contact

±2 kV, ±4 kV, ±8 kV,

±15 kV air

| ±8 kV contact

±2 kV, ±4 kV, ±8 kV,

±15 kV air

| Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30 %.
Electrical fast transient/burst IEC 61000-4-4| ±2kV for power supply lines

±1 kV for Input/output lines

| ±2kV for power supply lines| Mains power quality should be that of a typical commercial or hospital environment.
Voltage dips, short interruptions, and voltage variations on power supply input

lines IEC 61000-4-11.

| <5 % UT

(>95% dip in UT.) for 0.5 cycle

<5 % UT

(>95% dip in UT) for 1 cycle

70% UT

(30% dip in UT) for 25/30 cycles

<5% UT

(>95 % dip in UT) for 5/6 sec

| <5 % UT

(>95% dip in UT.) for 0.5 cycle

<5 % UT

(>95% dip in UT) for 1 cycle

70% UT

(30% dip in UT) for 25/30 cycles

<5% UT

(>95 % dip in UT) for 5/6 sec

| Mains power quality should be that of a typical commercial or hospital environment. If the user of the models P01 and P05 requires continued operation during power mains interruptions, it is recommended that the models P01, and P05 be powered from an uninterruptible power supply or a battery.
Power frequency (50/60 Hz) magnetic field lEC 61000-4-8| 30 A/m| 30 A/m| Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial

or hospital environment.

NOTE UT is the a.c. mains voltage before application of the test level.
Conducted RF lEC 61000-4-6 Radiated RF lEC 61000-4-3| 3 Vrms 150 kHz to 80 MHz 6 Vrms in ISM and amateur radio bands

10 V/m

80 MHz to 2.7 GHz.

385MHz- 5785MHz

Test specifications for

ENCLOSURE PORT IMMUNITY to RF

wireless communication equipment (Refer to table 9 of IEC 60601-

1-2:2014)

| 3 Vrms 150 kHz to 80 MHz 6 Vrms in ISM and amateur radio bands

10 V/m

80 MHz to 2.7 GHz

385MHz- 5785MHz Test

specifications for ENCLOSURE PORT IMMUNITY to RF

wireless communication equipment (Refer to Table 9 of IEC 60601-1-2:2014)

| Portable and mobile RF communications equipment should be used no closer to any part of the models P01, P05 including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.

Recommended separation distance d=[3,5/V1]×P1/2 d=1.2×P1/2 80 MHz to 800 MHz

d=2.3×P1/2 800 MHz to

2.7 GHz

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. b Interference may occur In the vicinity of equipment marked with the following symbol:

---|---|---|---

  • 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. Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcasts and TV broadcasts 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 model P08M is used exceeds the applicable RF compliance level above, the model P08M should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the model P08M.

  • b. Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3V/m.

  • Recommended separation distances between portable and mobile RF communications equipment and the model P08M

  • The model P08M is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the model P08M can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the model P08M is recommended below, according to the maximum output power of the communications equipment.

Rated maximum output power of the transmitter (W)

  • Separation distance according to frequency of transmitter m
  • 150 kHz to 80 MHz d=1.2×P1/2
  • 80 MHz to 800 MHz d=1.2×P1/2
  • 800 MHz to 2.7 GHz d=2.3×P1/2
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) 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) accordable 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.
  • Pressure Care Experts
  • Edward House, 5 Penner Road, Havant, PO9 1QZ
  • 02394 318 318
  • ask@oska.uk.com
  • oska.uk.com

Documents / Resources

| OSKA Dynaform Alternating Air Cushion [pdf] User Guide
Dynaform Alternating Air Cushion, Dynaform, Alternating Air Cushion, Air Cushion, Cushion
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References

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