4
Technical data
Power consumption at rest:
Approx. 2
A
Power consumption at transmitting
Approx. 40mA (GewaLink channel)
Input control switch type:
3.5mm jack plug 2-pole
Battery life:
Approx. 2 years (100 seconds transmitting per day with
GewaLink channel)
Programming locations:
4 places (Medi Easy) 28 places (Medi Standard)
Operating force buttons:
< 160g
Range:
40-50 m (GewaLink channels)
EMC-standard emission:
” immunity:
EN 301 489-3 V1.4.1:2002, EN(IEC) 61000-6-2:2005,
EN(IEC) 61000-6-3:2007, selected parts from EN 300
220-2 V2.3.1:2010
Computer Connection:
Via 429252 Control Tool USB interface
Measurements (L x W x H):
100 x 55 x 22 mm (incl. rubber feet)
Weight (incl. batteries):
105g
Operating temperature (excl.
batteries):
-20
C to +45
C
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 its 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.
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.
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.