CEN/TR 17223:2018


Status:
Gældende
Type:
Standard
Sprog:
Kategori:

Beskrivelse

This Technical Report provides guidance on the relationship between the requirements in the European Regulations for Medical Device and In Vitro Diagnostic Medical Devices and EN ISO 13485:2016 – Medical devices – Quality management systems – Requirements for regulatory purposes.

Antal sider: 0

Udgivet: 2018-03-21

Internationale relationer :

Varenummer: M315733


Udvalg og komiteer

Komite

  • CENCLC/JTC 3

Dansk udvalg

DS/S-257