Introduction: The Oxford/Hoyer Advance Patient Lift - Sunrise Medical Oxford Advance Manual De Instrucciones Y Garantía Para El Usuario

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INTRODUCTION: THE OXFORD/HOYER ADVANCE PATIENT LIFT

ABOUT YOUR LIFT
Statement of Intended Use:
The intended use of the lifting device is to transfer an individual from one resting sur-
face to another (such as a bed to a wheelchair). Moving a person in a sling over ANY
distance is not recommended.
The Oxford/Hoyer Advance is available in two versions, hydraulically operated and elec-
trically operated. This manual covers both Advance models. Each lift is fully assembled,
load tested and certified before being packed/shipped.
The packing consists of a strong, purpose built carton and is used for both export and
domestic markets to ensure the safe arrival of the lift. A number of documents are sup-
plied in a wallet packed with each lift and should be kept safely for future reference.
TEST CERTIFICATE
•
DEALER GUARANTEE CARD
•
The TEST CERTIFICATE is an important document and should be kept for reference pur-
poses. To properly maintain your lift please refer to the maintenance schedule included
in this document. If you are at all unsure what your local market servicing require-
ments are, please check with your dealer and/or a local government agency.
The Oxford/Hoyer Advance is suitable for the following CATEGORIES of lift within the
working parameters of the lifts specified in the TECHNICAL SPECIFICATIONS.
Category A - Wheelchair
Category B - Bed
Category C - Bath (dependent upon setting)
Category D - Toilet/Shower Chair
Category E - Floor
Category F - 90 degree Rotation
The Oxford/Hoyer Advance is suitable for patients in the SITTING, SITTING/RECUMBENT
and RECUMBENT positions. The slings suitable for this device are listed as follows
Oxford/Hoyer Quick fit sling
Oxford/Hoyer Full back sling
Oxford/Hoyer Quick fit deluxe sling
Oxford/Hoyer Long seat sling
Oxford/Hoyer Access sling
The CE mark:
294000.10003 Rev. A
USER MANUAL
•
CUSTOMER SATISFACTION CARD
•
The Oxford/Hoyer Advance carries the CE mark and complies
with the following EC directives:
• Medical Device Directive (93/42/EEC)
• EMC Directive (89/336/EEC) (Electrics only)
• Low Voltage Directive (73/23/EEC) (Electrics only)
E n g l i s h