Saagha SAS

• Agence Nationale de Sécurité du Médicament et des Produits de Santé
  FranceContacter l’autorité →

Aucun certificat enregistré pour ce fabricant.

Aucun dispositif enregistré pour ce fabricant.

2 contacts identifiés

• RM
  ROBERT Marylise

  PCVRR
  Voir le profil →
• ROBERT Marylise
  According to REGULATION EU 2017/745: - the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released; - the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; - the post-market surveillance obligations and reporting obligation are fulfilled; - in the case of investigational devices:compliance of the required statement.
  Masqué

• Saagha — FR-IM-000050681
• Saagha — FR-MF-000047047
• ROBERT Marylise — Saagha