PDR-7000 Operation Manual
SAFETY INFORMATION
Accessory equipment connected to the analog and digital interfaces must be certificated
according to the respective IEC standards (e.g. IEC 60950-1 for data processing
equipment and IEC 60601-1 for medical equipment). Furthermore all configurations shall
comply with the system standard EN 60601-1:2006, Clause 16. 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 IEC 601-1-1. If in doubt, consult the technical service department or your
local representative.
For U.S.A
Do not make any changes or modifications to the equipment unless otherwise specified in
the manual.
If such changes or modifications should be made, you could be required to stop operation
of the equipment.
For EU Countries
The following mark, the name & address of the EU Representative shows compliance of
the instrument with Directive 93/42/EEC.
Authorized Representative:
Medical Device Safety Service GmbH
Schiffgraben 41, D-30175
Hannover, Germany
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