MDT Int'l SA

• Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten
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• HUNTER Neil
  Art.15(3): a) the conformity of the devices is appropriately checked, in accordance with the QMS under which the devices are manufactured, before a device is released; b) the Technical Files and the EU DoC are drawn up and kept up-to-date; c) the PMS obligations are complied with in accordance with Art.10(10); d) the reporting obligations referred to in Art. 87 to 91 are fulfilled; e) in the case of investigational devices, the statement referred to in Section 4.1 of Chap.II of Ann.XV is issued.
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Dispositifs placés dans 16 pays

• Tchéquie5
• Pologne5
• Espagne4
• Italie4
• Slovaquie4
• Hongrie3
• Portugal3
• Autriche2
• Estonie2
• Lituanie2
• Lettonie2
• Allemagne1
• Grèce1
• Irlande1
• Turquie1
• XI1

• QbD RepS BV — représente — MDT
• HUNTER Neil — MDT