41
9. Safety and responsibility
Abilia has conducted a risk analysis for the product with reference to SS-EN 14971 for
Medical equipment. The instructions for use and the technical specifications for the product
have been drawn up in respect of the safety assessments carried out in this document.
It is always important to be aware of safety when first using this product and with it’s
subsequent use. It is not possible to describe in the instructions all the situations in which
the product must not be used. If you are not sure whether you have started using the
product properly or set it up correctly, please contact your supplier.
Abilia is not liable for any loss, damage or consequential loss resulting from any use, correct
or otherwise, lack of follow-up, incorrect set-up, incorrect connection or similar misuse.
Abilia financial liability is at all times limited to the value of the product itself.
9.1 Recycling Waste Electrical and Electronic Equipment
The Control Medi contains electronics components that must be recycled.
When the product is no longer of use, hand it in to a recycling centre for waste
electrical and electronic equipment.
9.2 Conformity with the Medical Devices Directive
The Control Medi is marketed as a technical aid for people with disabilities and meets the
requirements in the Medical Devices Directive 93/42/EEC including relevant EMC and
electrical safety requirements.
