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CR Reader, CR Advanced Reader, CR Multiformat Reader | Introduction to CR Reader,
CR Advanced Reader and CR Multiformat Reader | 21
Compatibility
The equipment must only be used in combination with other equipment or
components if these are expressly recognized by Agfa as compatible. A list of
such equipment and components is available from Agfa service on request.
Changes or additions to the equipment must only be carried out by persons
authorized to do so by Agfa. Such changes must comply with best engineering
practices and all applicable laws and regulations that have the force of law
within the jurisdiction of the hospital.
Accessory equipment connected to any interfaces must be certified according
to the respective IEC standards (e.g. IEC 60950 / IEC 62368-1 for data
processing equipment or IEC 60601-1 for medical equipment). Furthermore
all configurations shall comply with the requirements for ME systems
according to IEC 60601-1. 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 for ME
systems according to IEC 60601-1. If in doubt, consult your local service
organization.
2591D EN 20191028 1712
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