
Oxford®
Smart Monitor
3
English
1. Introduction: About Your Product
Please ensure you take time to read this manual thoroughly before using your Oxford Smart
Monitor. This will help ensure both patient and carer remain safe and free from injury throughout
the lifting and transfer process as well as to familiarise yourself with the product’s features and
functions.
If you are unsure on the use of this product or any specific element, please contact your local
authorised service provider or Joerns Healthcare for further advice.
WARNING
Do not attempt to use the Oxford Smart Monitor without first understanding this manual.
The CE Mark: The Oxford Smart Monitor 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)
Statement of Intended Use
The Oxford Smart Monitor is a control system for Oxford patient lifts. It stores useful servicing
information about the lift that can be recalled when required. This servicing information includes:
• Number of patient lift cycles
• Total work done by actuator
• Number of lift overloads (attempted lifts above the safe working load)
• Number of days since last service interval
The Smart monitor replaces the existing control box and is fully compatible and retro-fitable to
the following Oxford patient lifts (manufactured post 2003), fitted with a Linak actuator:
• Oxford Mini • Oxford Journey • Oxford Presence
• Oxford Midi • Oxford Elevate • Oxford Calibre
• Oxford Major • Oxford Ascend • Oxford Advance
• Oxford Maxi
For products not listed above, please consult Joerns Healthcare to verify and confirm
compatibility.
WARNING
DO NOT attempt to install a Smart Monitor Control box on a lift that is not listed above
without consulting Joerns Healthcare for advice.
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.