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prEN 389

Labelling of non-active medical devices prEN 389

General information

40.20   DIS ballot initiated: 12 weeks   Aug 12, 1990

CEN

CEN/TC 205 Non-active medical devices

European Norm

Scope

Will specify the minimum labelling requirements for non-active medical devices, including custom-made devices and devices for clinical evaluation

Life cycle

NOW

IN_DEVELOPMENT
prEN 389
40.20 DIS ballot initiated: 12 weeks
Aug 12, 1990




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