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ABPM with custo screen 100/200 and custo diagnostic | GEB 0141 – DK 0953 | Version 002 – 05.06.2013 | custo med GmbH
02
Safety notes
02.1
General
Strict compliance with the safety notes protects against personal injury and
property damage during device operation. This Operating Manual is designed
to accompany the product and should be kept ready to hand close to the
device. As either the operator or user of this device you should have read and
understood this Operating Manual, in particular the safety notes.
Laws and regulations applicable to the product
This system is designed in accordance with Medical Device Directive 93/42/EEC,
Class II a, and meets the requirements of protection class I or II (depending on
the power supply unit used; the recorder is a device with an internal power
supply), type BF according to DIN EN 60601-1.
Other devices which are part of the system must meet the requirements of
the office equipment standard (IEC 60950) and the standard for electromedical
devices (IEC 60601-1).
The electrical installations in the rooms in which the system is used must meet the
requirements of the applicable safety standards.
For users outside of Germany, the respective national accident prevention
measures, regulations and requirements apply.