English
1. Introduction
The Oxford Up is an assistive standing and transfer device, designed for moving a person over short
distances. This might be from bed to chair, chair to wheelchair or to and from a toilet/commode, for
example. The Up has a compact footprint, enabling effective use, even in confined spaces.
The packing consists of a strong, purpose built carton that is used for both export and domestic
markets to ensure the safe arrival of the product.
To properly maintain your product please refer to the maintenance schedule included in this
document. If you are at all unsure what your country's servicing requirements are, please check
with your authorised distributor and/or a local government agency.
The CE mark:
Statement of Intended Use
The Oxford Up is intended for use by an individual who has the ability to stand unassisted or with
minimal assistance. It will enable their transfer from one resting surface to another, such as from
a bed to a chair. It is an active product for users who can contribute effort to the standing and
transfer process. By encouraging user participation, the Up can be a valuable rehabilitation aid,
improving natural function and tone. The Up is designed for indoor use and for transfers on flat
surfaces, over short distances only.
Expected Service Life
Oxford Professional products are designed and tested for a minimum service life of ten (10)
years, subject to the use and maintenance procedures stated in this manual. Use, other than in
accordance with these instructions, may compromise service life.
Serious Incident Reporting
In the event of a serious incident taking place during use of this product, affecting the patient
and/or care-giver, it must be reported to the product manufacturer or authorised distributor.
Should the incident take place within the European Union (EU), it must also be reported to the
local competent authority within the member state. Please contact Joerns Healthcare in the first
instance for advice and guidance.
The Oxford Up carries the CE mark and complies with the following EC
directives:
• Medical Device Directive MDR 2017/745
Oxford
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Up
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