prEN 389

Labelling of non-active medical devices prEN 389

General information

Current stage: 40.20 DIS ballot initiated: 12 weeks Aug 16, 1990

Originator: CEN

Owner: CEN/TC 205 Non-active medical devices

Type: European Norm

Scope

This European Standard specifies minimum labelling requirements for non-active medical devices as defined in CEC Directive; including custom-made devices and devices for clinical evaluation

Life cycle

NOW

IN_DEVELOPMENT
prEN 389
40.20 DIS ballot initiated: 12 weeks
Aug 16, 1990