•
Not suitable for use in an Outdoor Environment.
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Do not connect to any other medical device or equipment.
•
The System should be cleaned after use or between patients. Refer to the Cleaning section.
•
Do not use bleach, phenols, chlorine based products which exceed 1000ppm available chlorine, solvents or alcohol based cleaners.
•
Do not immerse the Control Unit in water or other fluids.
•
Do not autoclave any parts of the Mercury Advance Mattress System.
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The system is not suitable for sterilisation.
•
Before cleaning make sure that the Control Unit is disconnected from the mains electricity supply.
•
Only qualified technicians trained or formally approved by DHG in the operation and maintenance of DHG products may carry out maintenance,
modification or repair work on the equipment. Unqualified personnel attempting to work on DHG Control Units risk serious injury to themselves
and others and possibly death by electrocution.
•
Inlet fuse NOT to be replaced by operator or patient, to be replaced by service personnel only.
•
Correct fuse rating MUST be used. Failure to do so could result in the risk of a fire.
•
Modification of this product in any way without authorization from DHG is strongly prohibited.
Cautions
•
It is recommended that an audit of all mattresses is carried out at least annually.
•
Mattresses can become damaged if stored incorrectly. Mattresses should be stored in a clean and dry environment.
•
It is not advised that mattresses are stored near heating devices, such as electrical fires or radiators.
•
Take care when handling the mattress to prevent damaging the cover or foam.
•
Avoid contact with abrasive surfaces, and do not drag the mattress.
•
Use of detachable parts not listed is not recommended by DHG.
All the above warnings and cautions together with safety considerations should be observed at ALL times during use of the Mercury Advance
Mattress System.
6. Serious Incidents
Any serious incident that has occurred in relation to the Dyna-Form Mercury Advance system should be reported to DHG or the Authorised
Representative and the Competent Authority of the country in which the user and/or patient is established.
7.Symbols
General Symbols
Read the user manual
Medical device
Class IIa product conforming to the requirements of
UK MDR 2002 for Medical Devices, MDD 93/42/EEC
General warning symbol
Temperature limitation
Humidity limitation
5
Atmospheric pressure limitation
Protect from heat and radioactive sources
IFU
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