opera Relieve Overlay Mattress System Instruction Manual
- June 3, 2024
- opera
Table of Contents
- Relieve Overlay Mattress System
- Explanation of Symbols
- Safety Precautions
- Warnings
- System Package
- Power Unit Features
- Mattress and Power Unit Installations
- Program Settings
- Patient Transfer and Transport
- Emergency CPR Deflation
- Cleaning Instruction
- Routine Maintenance and Storage
- Troubleshooting
- Return for Service
- Warranty
- Product Specifications
- Documents / Resources
OPERA® RELIEVE OVERLAY
MATTRESS SYSTEM
Instructions and Technical Specifications
Enhancing Lives, Delivering Comfort
Relieve Overlay Mattress System
Indications
This air alternating mattress system is designed for patients who endure
pressure ulcer and potential patients who wish to reduce the likelihood of
pressure ulcer.
This device is intended to treat and prevent pressure ulcers by facilitating
blood circulation and decreasing pressure of each tissues contact area. Always
consult a physician or healthcare professional before using this mattress
system. This anti-decubitus mattress system is mainly for medium risk patient
group.
Contradictions
Certain patient conditions are not suitable for using this type of device such
as fracture of unstable vertebrae and illness of unstable vertebrae. Always
consult a physician or health professional before using this device.
The use of this system does not replace the regular repositioning, monitoring
and, nursing of the patient.
****Thank you for purchasing this anti-decubitus mattress replacement system.
Please read these instructions carefully before setting up and using the
device. Pay special attention to the warnings and other safety information.
Use of genuine components is essential for optimal performance. If you do not
fully understand all the instructions, safety precautions, and warnings, do
not use this device. If you have questions, please contact Opera on 0333 222
8584.
Explanation of Symbols
| Read information with this symbol carefully and urgently follow
instructions. This information is safety-relevant.
---|---
DANGER
| This symbol indicates general hazards. There is danger to life and health.
| Conformity mark in accordance with the Medical Device Directives 93/42 EEC.
IPX0
| Do not immerse power unit in liquid or spray liquids directly on power
unit.
| Double Insulated (Class II) equipment.
| Symbol for type B device according to DIN EN 60601-1.
| Indoor use only.
| This product must be disposed of in a separate refuse collection in the
European Union. Do not dispose of as normal domestic waste.
| Read instructions.
****| Manufacturer.
| Date of Manufacture.
Safety Precautions
2.1 Proper Operation
To ensure proper operation, please inspect and verify that all parts are set
up properly and are anchored securely to the bed system. Verify that the
mattress replacement system does not interfere with the bed frame function. Do
not place anything on top of the power unit. Make sure power cord set is
underneath the bed frame and does not pose a hazard.
2.2 Use of Linens
It is recommended to limit bed linens to a single layer in order to allow
moisture to escape efficiently through the coverlet. Breathable incontinent
pads are recommended for use with this mattress system.
2.3 Flammability Hazard
**Avoid using this device near open flames, lighters, or cigarettes.
Flammability hazard exists. This device draws air from the surrounding
environment. Thus, cigarette smoking may damage internal components.
2.4 Disinfection Between Patients
This system should be disinfected thoroughly between patients in order to
avoid cross contamination.
2.5 Weight Capacity**
Verify that the patient’s weight, accessories, and this mattress replacement
system, do not exceed the bed frame’s manufacturer’s recommended weight
capacity.
Warnings
3.1 Side Rails
**Use this mattress with side rails that meet bed rail regulations (BS EN
60601-2-52:2010) to ensure that the gap between the side rail and the top of
the mattress is not large enough to pose risk of head or neck entrapment.
Failure to do so could result in serious patient injury or death. If
applicable, adhere to facility or local guidelines regarding entrapment
regulations.
3.2 Do Not Disassemble
**Do not disassemble the power unit if you are not a qualified technician.
Please contact Opera on 0333 222 8584.
3.3 AP/APG Protection
This product is not AP/APG protected.
3.4 Periodic Repositioning
It is recommended that the patient be repositioned periodically while using
this mattress.
3.5 Maintenance
If the equipment needs maintenance, contact Opera on 0333 222 8584 as soon as
possible. For equipment that is no longer functional, make sure to follow
national, state, and/or facility requirements for disposal of the unit.
3.6 Maximum Operating Temperature
The air mattress operates at a maximum temperature of 100 °F (37.7 °C).
3.7 Sharp Protrusions
**Ensure that there are no protruding objects, sharp points, or bed springs
under the mattress as these could puncture the air cells.
3.8 Disposal of Waste**
This device must not be disposed of as normal household waste after the end of
its service life. Contact your local waste recycling facility for further
instructions.
System Package
4.1 Power Unit Package
Power Unit x 1
Power Cord x 1
Instructions For Use x 1
4.2 Mattress Package
Mattress replacement unit with coverlet x 1.
Power Unit Features
a. Power Switch
The green power LED will light when the main power rocker switch on the panel
is turned on.
b. Lockable Patient Weight Knob
Patient Weight Knob is used to adjust the internal pressure of the mattress
according to patient weight. Simply turn the knob to adjust the pressure
setting if the mattress is too soft or firm to suit each patient’s needs.
Caregivers should always perform a hand check by placing their hands
underneath the patient’s pelvis area to check if there is sufficient air
support to ensure that the patient is not bottoming out.
c. Couplers
Quick release female couplers are used to secure mattress air hoses to the
power unit.
d. Strain Relief of Power Cord
Provided with a moulded-on anti-kink bushing held in place by integral slot in
bottom enclosure.
e. Hanging Hooks
Hanging hooks are designed to hang the power unit on almost any foot board.
f. Air Filter and Cap
We recommend that the filter is kept clean to ensure optimal performance of
the power unit.
g. Fuse
Fuse Holder
Mattress and Power Unit Installations
6.1 Secure Mattress Overlay
Place mattress overlay on top of the original mattress with the logo at the
foot end. Secure the mattress using the elastic straps at four corners. Please
verify all bed functions are working properly without interference before
proceeding to the next step. Also, check the combined height of the Overlay
and Mattress meets bed rail regulations (BS EN 60601-2-52:2010).
6.2 Secure Power Unit
Secure the power unit on to the foot board using hanging hooks.
6.3 Connect Hose Couplers
Firmly connect the air hose couplers to the couplers on the power unit.
6.4 Power Up Unit
Plug the power unit into an electrical outlet, and turn on the main power
rocker switch on the control panel.
6.5 Set Patient Weight
Turn the lockable patient weight knob on the power unit’s control panel to
maximum setting to shorten the initial inflation time if needed.
6.6 Wait for Inflation
Wait approximately 30 minutes for the mattress to inflate fully before
allowing the patient to lie down on the mattress.
Program Settings
7.1 Adjusting Firmness
Place the patient in the centre of the mattress. Adjust the mattress’ internal
pressure according to the patient weight by using the lockable patient weight
knob on the control panel of the power unit. If the mattress is too soft or
too firm, increase or decrease the mattress’ internal pressure one increment
at a time and wait for the system to stabilise before making another change.
Continue this process until comfort is achieved.
7.2 Perform Hand Check
Caregivers should always perform a hand check by placing their hands
underneath the patient’s pelvis area to check if there is sufficient air
support to ensure the patient is not bottoming out.
****Tucking the bed sheet in too tightly may reduce the effectiveness of the
system.
Patient Transfer and Transport
8.1 Transfer
It is recommended to have the mattress system fully inflated during the
transfer process. Make sure the bed is secured before proceeding.
8.2 Transport
In the event of a patient transport, two options are available.
- Detach the mattress’ air hose couplers from the power unit’s quick release couplers and connect the two air hose couplers together to retain air in the mattress. The mattress will stay inflated for approximately 2 hours, depending on the patient’s weight.
- Unplug the power unit’s power cord from the wall outlet and the mattress should stay inflated for approximately 40 – 50 minutes. This mattress system also has a safety foam base underneath the air cells to support the patient for a short period of time in case of deflation. To resume normal operation, please follow the instructions beginning in Section 6.1.
Emergency CPR Deflation
DANGER
In the case of emergency, pull on the air hose couplers from the control
unit and turn off the power unit by pressing the power/mute button on the
control panel at the same time for emergency deflation. The air will discharge
from the mattress with the patient’s own weight. To resume normal operation,
simply re-insert the air hose couplers, press the power/ mute button again and
reset the patient weight. See instructions in Section 6.1.
Cleaning Instruction
The air mattress and power unit must be cleaned thoroughly between patients to
avoid cross contamination. The following is a suggested guideline. Be sure to
follow local infection control policies.
Regular cleaning can be performed at bedside with a disinfectant followed by
drying with a clean dry cloth. Use only mild detergents to clean the coverlet
and the mattress. Any appropriate non-phenolic cleaning agent may be used for
heavy soiling from urine, blood or other bodily fluids. Please ensure that the
air mattress and coverlet are completely dry before letting the patient lie on
the surface again.
Machine wash warm water at maximum 71 °C.
Do not use electric or tumble dryers. Do not iron.
Always unplug the power unit before cleaning. Routine cleaning of power unit
can be done by wiping down with damp cloth using disinfectant or mild
detergent. Never spray liquids directly on the unit itself.
Routine Maintenance and Storage
Remove air filter from the rear panel of the power unit by opening up the
filter cap. Inspect the filter for dirt or dust, and clean it with mild soap
and water.
Reinsert the dried air filter after cleaning and ensure that the cap is
secure. If a replacement is needed, contact Opera on 0333 222 8584.
Only disinfected and dry systems should be stored. Disconnect the air hoses
from the power unit. Roll up the mattress starting from the head end and
working down toward the foot end. Use the straps to secure it and store in
clean plastic or other storage bag. Store in a cool, dark place.
Troubleshooting
Fault | Inspection Procedure | Remedy |
---|---|---|
Power unit is not working | Check if power cord is firmly plugged into both the |
control
unit and the electrical outlet.| Secure power cord into control unit and/or
electrical outlet.
Check if the power switch is inthe on position.| Turn power switch to on
position.
Check if the power surge has shut down the power unit.| A power surge may
overload the circuitry temporarily. Turn the unit off, and check the fuse for
damage. Turn the unit on again with normal procedure.
Make sure there is no power failure.| Turn on and operate the unit after power
is restored to the
facility or home.
Power unit does not respond to possible solutions.| Please contact Opera on
0333 222 8584 for assistance.
Power unit is working, but mattress replacement is not
inflating
and/or
Bottoming out is occurring
and/or
Patient leaves a
deep indentation at the
contact area which does
not return back to its
original shape.| Check CPR Pull Cord.| Unzip mattress cover and inspect CPR
latch is fully inserted into socket.
Check if mattress’ air hose couplers are properly connected to power unit’s
quick release couplers.| Secure air hose couplers firmly into place.
Verify that patient weight setting is correct.| Increase or decrease weight
setting until appropriate pressure is reached.
Inspect air filter for dust and dirt.| Clean or replace air filter.
Lift mattress coverlet up to check if air cells are connected correctly.| Make
sure all air cells are properly linked to air supply.
Lift mattress coverlet up to check if air tubes are kinked or
obstructed.| Check and adjust air tubes positions.
Check if air cells are cut or cracked| Please contact Opera on 0333 222 8584
for assistance.
Patient’s wounds are not responding to pressure relief
(reddening of skin).| .| Contact your physician and/or nursing service
immediately.
Return for Service
Service and repair must be performed by Opera authorised technicians or representatives. Please contact Opera on 0333 222 8584.
Warranty
We warrant the product to be free from defects from the date of purchase.
Please inspect all accessories when you purchase our product. If there is any
damage or missing accessories when you receive the product, please ask for a
replacement from Opera on 0333 222 8584 within three days of purchase.
The warranty period for the products are according to the regulations in your
country, the minimum period is 2 years from date of purchase for the power
unit and 2 years for the mattress and the coverlet. The warranty coverage of
any product is contingent up on its purchase from Opera.
Warranty coverage will not be extended to any product on which the production
lot number has been removed or defaced on which repair has been attempted by
any person or agency not authorized by our company or if in the sole opinion
of our company that the system shows evidence of tampering, abnormal or
unreasonable abuse, negligence, accident or operation without regard for the
restrictions specified in the instructions which accompany the system. This
warranty does not cover normal maintenance such as cleaning, adjustment,
lubrication, and updating of equipment or parts. If the damage is a result
from improper operation, a reasonable service fee and part cost will be
charged. The warranty stated above is the only warranty made and is in lieu of
all other warranties whether expressed or implied, including any warranty of
merchantability or fitness for a particular reason, we will not be liable for
consequential or incidental damages of any kind.
Product Specifications
System Name | RELIEVE Overlay Mattress System |
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Power Unit (Air Pump) Model | SR303 |
Mattress Dimension | 2000 x 900 x 130mm (5″ depth) |
Number of Air Cells | 16 Cells |
Power Control Unit Dimension | 260 x 220 x 90mm |
Material | Power Unit – Plastic Case rated UL 94V-0 |
Mattress Cell -100i° nylon with TPU lamination
Coverlet – Quilted Nylontaffeta Backing
Power Input| 220 – 240Vac, 50Hz, 0.05A
Power Consumption| Normal Operation: Max 6W
Power Control Unit Weight| 2.5 kg
Fuse Rating| T1A 250V
Electrical Classification| Class II Type B, double insulated.
IPXO, do not immerse power unit in any liquid, or spray any liquids directly
on the power unit.
This system is not AP/APG Protected.
Continuous operation.
Power Cord| HOWV-F or HO5VVH2-F, 2 x Min. 075mm2
Operating, Transportation & Storage Conditions| Temperature: 5°C – 40°C
Humidity:15% – 60%
Atmospheric Pressure: 700 – 1060hPA
IEC/EN Test Standards| Safety: IEC/EN 60601-1_v3.0
EMC: IEC/EN 60601-1-2_v3
Maximum Weight Capacity| 150 kg
Notes
……………………………….
Azure House, Connaught Road, Kingswood, Hull, HU7 3AP
0333 222 8584 |support@operabeds.com |
operabeds.com
Version 2 | Published in August 2022
Documents / Resources
|
opera Relieve Overlay Mattress
System
[pdf] Instruction Manual
Relieve Overlay Mattress System, Relieve Overlay System, Mattress System,
Overlay System, Relieve System
---|---
References
Read User Manual Online (PDF format)
Read User Manual Online (PDF format) >>