sidhil PLUS II Dynamic User Instructions

PLUS II Dynamic Mattress Replacement System User Instructions
www.sidhil.com
CONTENTS
Important Notice
Before operating this medical equipment, it is important to read this manual and understand the operating instructions and safety precautions. Failure to do so could result in injury and/or damage to the product.
If you have any questions, please see contact information on rear cover.
INTRODUCTION ..................................... 4
SAFETY PRECAUTIONS ......................... 5
PRODUCT OVERVIEW............................ 6
INSTALLATION ....................................... 7
OPERATION ............................................ 9
Control Unit Panel ................................ 9
Mattress Function ................................ 9
Use of Incontinence Products ............. 11
Static Mode ....................................... 11
Removal & Transport Function ............ 12
Mains Supply Power Failure ................ 12
TROUBLESHOOTING ........................... 13
CLEANING ............................................ 15
MAINTENANCE .................................... 16
TECHNICAL SPECIFICATION ................. 17
WARRANTY INFORMATION ................. 23
3
INTRODUCTION
Plus II Dynamic Mattress Replacement System
Thank you for choosing a Plus II Dynamic Mattress Replacement System. This user manual should be read carefully before using the mattress as it contains important information regarding safe operation and maintenance in order to provide long lasting and reliable service.
Please ensure that you understand all the instructions, if you have any questions concerning the operation and maintenance of the mattress please contact your supplier who will provide you with expert professional advice.
Plus II Mattress System
The box contains an assembled
mattress system consisting of:
A. Plus II Alternating Dynamic System
B. Digital Control Unit
C. Power Cord
D. Carry Bag
E. User Manual
C.
D. E.
A.
B.
4
SAFETY PRECAUTIONS
In General Control Unit
Do not use this equipment in the
presence of flammable anaesthetics.
Keep away from sources of heat and
naked flames.
Bed frames used with the systems
can vary greatly depending on the specific healthcare setting (i.e. hospitals, nursing homes, home care etc). It is the responsibility of the carer to carry out the necessary risk assessments to ensure the safety of the patient. This includes, but is not limited to, the appropriate use of side rails to prevent falls and/or patient entrapment.
Minimise articles (e.g. bedding) between
the mattress surface and patient, and secure bed sheets loosely so as not to affect the alternating cell movement.
The control unit is tested and CE marked in line with Medical Device Directive (93/42/ EEC).
Only plug into a mains socket using the mains cable supplied with the system.
Exposure of the control unit to any liquid while it is plugged in could result in a severe electrical hazard.
Only use fuses that have the same specified rating. Using fuses with higher ratings could result in damage and/or injury. (See Technical Specification).
The control unit is a precision electronic product. Use care when handling or transporting. Dropping or other sudden impacts may result in damage to the unit.
Do not open the control unit – risk of electrical shock. Do not attempt to repair or service the control unit. Repairs and service should be conducted by suitably trained personnel. If the control unit is not functioning properly, or has been damaged, unplug the unit and take it out of service immediately (See contact information on rear cover for repair and service information).
Do not place any objects or items, such as blankets, on or over the control unit.
The mains cable to the control unit should be correctly positioned to avoid a tripping hazard and/or damage to the cable. It is recommended to place the cable under the bed frame and attach it to a mains socket by the head end of the bed.
5
PRODUCT OVERVIEW
Alternating Mattress System (see Technical Specification)
The Plus II Dynamic Mattress Replacement System is intended to provide comfort and pressure relief to patients vulnerable to pressure damage. It is designed for use on both standard and profiling bed frames. Ideally, patients allocated to this system will have some degree of independent mobility or can be repositioned according to individual needs.
The maximum patient weight limit is
177kg (28 Stone).
Mattress
This system includes three static head cells to provide static support for optimum user comfort, while air pressure in the other cells is alternated over a 12 minute cycle. This provides regular periods of pressure reduction to aid blood and lymphatic flow to vulnerable tissue
Control Unit
The control unit provides the air supply to the mattress.
• It is controlled via a touch panel with integrated digital display. The alarm sounds when low pressure is detected or when power is interrupted. The alarm mute function silences the alarm for a maximum of 20 minutes – the alarm resumes if the cause of failure is not resolved. The alarm will sound for up to two hours following an interruption to power.
• The control unit includes a back up battery for the audible alarm. This battery is continuously re-charged and will last the life time of the product.
• Functions on the control panel adjust the 8 comfort level settings.
• When a fault condition exists a warning LED is illuminated with an audible alarm.
The visible and audible alarm function has a number of indications depending on the cause of the failure (see’Troubleshooting’ section).
If the mains cable becomes detached the alternation sequence is suspended and the mattress cells remain inflated and/or deflated based on the current cycle. The audible alarm
will sound.
6
INSTALLATION
Any damaged or missing components should be reported to your supplier as soon as possible.
System Installation Control Unit Activation
The following describes the procedures for initial system set up:
a. Remove all covers, sheets and mattress
from the bed.
b. On a standard bed, position the mattress
on top of the bed frame, top cover facing upwards and air hoses at the foot of the bed for control unit positioning.
c. Attach to the bed by securing the
adjustable straps loosely under each section of the bed.
On a profiling bed, secure the
adjustable straps around the moveable
sections of the bed frame.
d. To avoid any risk of damage to the mattress
ensure there are no sharp objects which may come in contact with it.
Check that the attachment of
the mattress does not interfere with the
movement or operation of the bed.
e. Ensure the CPR tag sealing connectors are
pushed firmly onto the air pipes.
a. Position the control unit by hanging the
hooks over the foot board or place unit on the floor under the bed with the front facing upwards. Ensure the rear of the unit is not obstructed by carpet, rugs etc. It is advisable to place the unit on a firm surface.
b. Attach the air connector handle to the
control unit. Ensure air hoses do not kink between frame and control unit.
c. Insert mains cable into the control unit, plug
into a mains socket.
Press the power button for at least two
d.
seconds to activate the control unit. pressure LED’s will flash indicating the system has activated. The system will be ready for use in a maximum of 50 minutes.
e. When initial inflation is complete, the 4th
pressure LED and the alternating mode LED will illuminate to indicate the system is ready for use (system automatically defaults to alternating mode at start-up)
f. Once inflated, ensure the straps that attach
the mattress to the bed frame are secure and hold the mattress in place, adjust as necessary.
g. Once the mattress is fully inflated, the
bedding can be replaced. Secure sheets loosely enough to ensure they do not interfere with cell alternation.
The
.
7
INSTALLATION
To attach the handle to the control unit:
1) Depress the lever on the top of the handle.
2) Aligning the ports on the handle with those on the control box, firmly push the handle into position.
3) Release the lever, ensuring this has engaged onto the catch connected to the control box.
To remove the handle from the control unit:
1) Depress the lever on the top of the handle.
2) Pull the handle away from the control unit.
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