
Equipment Classification
Per EN/IEC60601-1, Medical Electrical Equipment, General Requirements for
Safety 3rd Edition, the DR Detector is classified as following.
Class I equip-
ment
Equipment in which protection against electric shock does
not relay on basic insulation only, but includes a power sup-
ply cord with protective earth conductor. For earth reliabili-
ty always plug the main power cord into an earthed mains
power outlet.
Type B equip-
ment
A Type B piece of equipment is one that provides a particu-
lar degree of protection against electric shock particularly
regarding allowable leakage current and reliability of the
protective earth protection.
Water ingress IP53
This device is protected against spraying water.
Flammable
anesthetics
This device is not suitable for use in the presence of a flam-
mable anesthetic mixture with air, or in presence of a flam-
mable anesthetic mixture with oxygen or nitrous oxide.
Operation
Continuous operation.
Applied Parts
The DR Detector tube side is an applied part.
Expected serv-
ice life
Up to seven (7) years
(if regularly serviced and maintained according to Agfa in-
structions)
Non-medical equipment
Following components are classified as non-medical equipment:
• System Control Unit
• Workstation
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| DX-D 60C, DX-D 60G | Introduction to the DR Detector
0294B EN 20190221 1131