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SSH EN 60601-2-17:2004

Medical electrical equipment - Part 2-17: Particular requirements for the safety of automatically-controlled brachytherapy afterloading equipment

Sep 22, 2004
95.99 Withdrawal of Standard   Sep 10, 2024

General information

95.99     Sep 10, 2024

DPS

DPS/KT 215

European Norm

11.040.60     19.100  

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Scope

The use of afterloading equipment for brachytherapy purposes may expose patients to danger if the equipment fails to deliver the required dose to the patient, or if the equipment design does not satisfy standards of electrical and mechanical safety. The equipment may also cause danger to persons in the vicinity if the equipment itself fails to contain the radioactive source(s) adequately within the storage container(s) and/or if there are inadequacies in the design of the treatment room. This Particular Standard establishes requirements to be complied with by manufacturers in the design and construction of afterloading equipment for use in temporary brachytherapy procedures. Its purpose is to identify those features of design that are regarded, at the present time, as essential for the safe operation of such equipment. It places limits on the degradation of equipment performance beyond which it can be presumed that a fault condition exists and where an interlock then operates to return the radioactive source(s) to the storage container(s) and afterwards to prevent continued operation of the equipment.

Related directives

Directives related to this standards.

93/42/EEC

Medical devices

Harmonized

Life cycle

NOW

WITHDRAWN
SSH EN 60601-2-17:2004
95.99 Withdrawal of Standard
Sep 10, 2024

REVISED BY

PUBLISHED
SSH EN 60601-2-17:2015

Related project

Adopted from EN 60601-2-17:2004

Adopted from IEC 60601-2-17 Ed. 2.0 b