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+44 (0)1709 377172
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+44 (0)1709 377173
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sales@harvesthealthcare.co.uk
www.harvesthealthcare.co.uk
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7
GENERAL
INFORMATION
The
Duke System
is an alternating pressure relieving mattress system used in the prevention
and treatment of pressure ulcers, and is recommended for use by a patient who is at risk from
developing pressure sores. The mattress is fitted with a vapour permeable two way stretch
cover.
By using the established principles of alternating therapy, the
Duke System
offers the patient
comfortable and relaxing support that can both prevent tissue breakdown and enhance
healing.
The
Duke Pump
unit is lightweight and compact; its features include an audible and visual
low-pressure warning, intergrated battery backup and a manual pressure / comfort control
function.
The
Duke Mattress
is made up of 30 individual cells. 25 alternating air cells and 5 static cells
at the head end. The alternating cells are split into 2 sections - odd cells e.g. 1,3,5 etc and
even cells e.g. 2,4,6 etc. These two sections will alternate through a 10 minute cycle in which
time both sets of air cells will have inflated and deflated sequentially. All air cells are individually
replaceable should any damage occur.
The quick release 3 pipe connector complete with transport cap enables easy patient
transport arrangements. For rapid deflation of the system simply twist open the CPR.
The
Duke Extra Mattress
is based on the Duke Replacement Mattress System with an
additional foam surround, suitable for wider beds The mattress has 25 alternating air cells and
3 static cells at the head end. Available in 1200mm and 1370mm width, the mattresses have
an increased maximum weight limit of 50 stones / 317 kg. The surround is visco topped for
comfort and can be used on a profiling bed.
GENERAL INFORMATION
Read through this instruction manual conscientiously from start to finish.
Please note that the various safety instructions must be observed.
BEFORE USING THIS SYSTEM FOR THE FIRST TIME:
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-
Harvest Healthcare products bear the CE mark and meet all safety and functionality
requirements.
These safety requirements can only be met if the user is satisfied with the proper condition of
the product (including accessories) before use.
GENERAL
INFORMATION
1
DEFINITION OF THE GROUPS MENTIONED
OPERATOR
An operator is any natural or legal person who uses the equipment or on whose instruction
it is used (e.g. nursing homes, specialised retailers, health insurance companies, medical
suppliers).
USER / CARE PERSONNEL
Users are persons who as a result of their vocational training, experience or briefing are
authorised to operate the equipment.
Furthermore, the user/ care personnel can recognise and avoid potential dangers and assess
the clinical condition of the service user.
PATIENT / OCCUPANT / SERVICE USER
The person in need of care, handicapped or infirm.
QUALIFIED PERSONNEL
Qualified personnel are employees of the operator who as a result of their vocational
training or briefing are entitled to deliver, assemble, disassemble and transport the product.
2
NON-COMPLIANT USE
All uses deviating from the intended purpose, which may also be hazardous as a result.
This includes for example:
•
Incorrect installation.
•
Operation by persons who have not been instructed in its use.
•
Using the system with non-approved parts/accessories.
•
Using the system if any of the components are damaged or faulty.
3.1
GENERAL SAFETY INSTRUCTIONS
During the briefing, specific attention must be drawn to any potential dangers
which can occur despite correct operation. Before putting the product into service
for the first time, the Instruction Manual must be read conscientiously and in detail
by the user / care personnel.
3
SAFETY INSTRUCTIONS
