Ion Beam Applications S.A.

• Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten
  BelgiqueContacter l’autorité →

Dispositifs placés dans 11 pays

• Belgique1
• Allemagne1
• Danemark1
• Espagne1
• France1
• Italie1
• Pays-Bas1
• Pologne1
• Portugal1
• Suède1
• Turquie1

Aucun certificat enregistré pour ce fabricant.

6 contacts identifiés

• BV
  BURGUET Véronique

  PCVRR
  Voir le profil →
• WI
  WATHION Inez

  PCVRR
  Voir le profil →
• WR
  WICHERN Ronald

  PCVRR
  Voir le profil →
• BURGUET Véronique
  ensuring that (a) the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; (b) in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
  Masqué
• WATHION Inez
  for ensuring that (a) 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; (b) the post-market surveillance obligations are complied with in accordance with Article 10(10); (c) the reporting obligations referred to Articles 87 to 91 are fulfilled.
  Masqué
• WICHERN Ronald
  ensuring that (a) the conformity of the devices is checked, in accordance with the QMS under which the devices are manufactured, before its release; (b) the TD and the EU DoC are drawn up and kept up-to-date; (c) the PMS obligations are complied with in accordance with Article 10(10); (d) the reporting obligations referred to in Articles 87 to 91 are fulfilled; (e) in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
  Masqué

• IBA — BE-MF-000000818
• IBA — BE-PR-000050794
• BURGUET Véronique — IBA
• WATHION Inez — IBA
• WICHERN Ronald — IBA