0459 - NOTIFIED BODY (UNDER DIRECTIVE 93/42/EEC Medical devices)

Name and address of the notified bodie
Responsible for the following products
Responsable for the following procedures/modules
Annexes/articles of the directives

GROUPEMENT POUR L'EVALUATION DES DISPOSITIFS MEDICAUX
G-MED
33, avenue du Général Leclerc
F - 92260 Fontenay Aux Roses

T : 00 33 1 40 95 63 54
F : 00 33 1 40 95 62 43
URL :
Email :

All medical devices

 

I

Full quality assurance
Type-examination
EC verification
Production quality assurance
Product quality assurance

 

Annex II
Annex III
Annex IV
Annex V
Annex VI

 

0459 - NOTIFIED BODY (UNDER DIRECTIVE 90/385/EEC Active implantable medical devices)

Name and address of the notified bodie
Responsible for the following products
Responsable for the following procedures/modules
Annexes/articles of the directives

GROUPEMENT POUR L'EVALUATION DES DISPOSITIFS MEDICAUX
G-MED
33, avenue du Général Leclerc
F - 92260 Fontenay Aux Roses

T : 00 33 1 40 95 63 54
F : 00 33 1 40 95 62 43
URL :
Email :

All active implantable medical devices

Full quality assurance
Type-examination
EC verification
Production quality assurance

Annex II
Annex III
Annex IV
Annex V

0459 - NOTIFIED BODY (UNDER DIRECTIVE 98/79/EEC In Vitro Diagnostic Medical Devices )

Name and address of the notified bodie
Responsible for the following products
Responsable for the following procedures/modules
Annexes/articles of the directives

GROUPEMENT POUR L'EVALUATION DES DISPOSITIFS MEDICAUX
G-MED
33, avenue du Général Leclerc
F - 92260 Fontenay Aux Roses

T : 00 33 1 40 95 63 54
F : 00 33 1 40 95 62 43
URL :
Email :

In vitro diagnostic medical devices

 

 

EC declaration of conformity Full quality assurance system EC Type -examination EC verification production quality assurance

Annex III
Annex IV
Annex V
Annex VI
Annex VII

 

 


site - http://www.hosmat.fr - dernière mise à jour : 3 juillet 2002