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SAFETY INFORMATION
SAFETY INFORMATION
SAFETY INFORMATION
SAFETY INFORMATION
Accessory equipment connected to the analog and digital interfaces must be certificated
according to the respective IEC/EN standards (e.g. IEC/EN 60950 for data processing
equipment and IEC/EN 60601-1 for medical equipments).
Furthermore all configurations shall comply with the system standard EN 60601-1-2:2007.
Everybody who connects additional equipment to the signal input part or signal output part
configures a medical system, and is therefore responsible that the system complies with the
requirements of the system standard EN 60601-1-1:2001.
If in doubt, consult the technical service department or your local representative.
For EU Countries
The following mark, the name & address of the EU Representative shows compliance of the
instrument with Directive
Council Directive 93/42/EEC of 14 June 1993
as amended by
Directive 2007/47/EC
concerning medical devices.
BIOTEK s.r.l.
Via Golfo di Taranto,7
74100 Taranto, Italy
TEL:+39-99-7723019
FAX:+39-99-7723624
0120
