Allergan Industrie SAS

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

Devices placed in 31 countries

• Austria3
• Belgium3
• Bulgaria3
• Czechia3
• Germany3
• Denmark3
• Estonia3
• Spain3
• Finland3
• France3
• Greece3
• Croatia3
• Hungary3
• Ireland3
• Iceland3
• Italy3
• Liechtenstein3
• Lithuania3
• Luxembourg3
• Latvia3
• Malta3
• Netherlands3
• Norway3
• Poland3
• Portugal3
• Romania3
• Sweden3
• Slovenia3
• Slovakia3
• Türkiye3
• XI3

No certificates registered for this manufacturer.

6 contacts identified

• GA
  GIACOMINI Annie

  PRRC
  View profile →
• PV
  PERRIN Véronique

  PRRC
  View profile →
• TE
  TEYROUZ Emilien

  PRRC
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• GIACOMINI Annie
  In the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
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• TEYROUZ Emilien
  - 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 post-market surveillance obligations are complied with in accordance with Article 10 (10), - the reporting obligations referred to in Articles 87 to 91 are fulfilled.
  Hidden
• PERRIN Véronique
  The technical documentation and EU declaration of conformity are drawn-up and kept up-to-date,
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• Allergan — FR-MF-000000490
• Allergan — FR-PR-000000489
• GIACOMINI Annie — Allergan
• PERRIN Véronique — Allergan
• TEYROUZ Emilien — Allergan