Keri Medical SA

• Agence Nationale de Sécurité du Médicament et des Produits de Santé
  FranceContact the authority →

Devices placed in 31 countries

• France225
• Belgium220
• Italy220
• Poland220
• Austria217
• Czechia217
• Germany217
• Denmark217
• Finland217
• Greece217
• Hungary217
• Luxembourg217
• Netherlands217
• Norway217
• XI217
• Lithuania216
• Spain215
• Ireland215
• Sweden215
• Estonia213
• Latvia213
• Portugal213
• Slovenia213
• Slovakia213
• Croatia205
• Bulgaria201
• Cyprus189
• Romania175
• Türkiye166
• Malta165
• Liechtenstein2

6 contacts identified

• MC
  PRRC
• MJ
  PRRC
• PB
  PRRC
• MOTTET Julie
  The technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. The post-market surveillance obligations are complied with. The reporting obligations are fulfilled. In the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
  Hidden
• PRANDI Bernard
  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 are complied with. The reporting obligations are fulfilled. In the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
  Hidden
• MILETTO Camille
  The technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. The post-market surveillance obligations are complied with. The reporting obligations are fulfilled.

• Intertek Medical Notified Body AB — 3 certificates — Keri Medical SA
• Keri Medical France — represents — Keri Medical SA
• MILETTO Camille — Keri Medical SA
• MOTTET Julie — Keri Medical SA
• PRANDI Bernard — Keri Medical SA