TEKNIMED SAS

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

Dispositifs placés dans 26 pays

• Autriche92
• Belgique92
• Chypre92
• Allemagne92
• Finlande92
• France92
• Irlande92
• Islande92
• Malte92
• Pays-Bas92
• Espagne91
• Italie83
• Bulgarie12
• Tchéquie12
• Grèce12
• Pologne11
• Portugal11
• Hongrie10
• Lituanie10
• Roumanie9
• Lettonie8
• Croatie7
• XI5
• Estonie4
• Slovaquie3
• Luxembourg1

Aucun certificat enregistré pour ce fabricant.

4 contacts identifiés

• SS
  SALLES Stéphanie

  PCVRR
  Voir le profil →
• VD
  VAN DE MOORTELE Solange

  PCVRR
  Voir le profil →
• SALLES Stéphanie
  - Person responsible for ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. - Person responsible for ensuring that 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. - Person responsible for ensuring that the reporting obligations referred to in Articles 87 to 91 of MDR (EU) 2017 /745 are fulfilled.
  Masqué
• VAN DE MOORTELE Solange
  - Person responsible for ensuring that the post-market surveillance obligations are complied with Article 10(10) of MDR (EU) 2017/745. - Person responsible for ensuring that for investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
  Masqué

• TEKNIMED SAS — FR-IM-000001225
• TEKNIMED SAS — FR-MF-000001224
• TEKNIMED SAS — FR-PR-000001226
• SALLES Stéphanie — TEKNIMED SAS
• VAN DE MOORTELE Solange — TEKNIMED SAS