MEDITEC DEVICES

• Danish Medicines Agency, Pharmacovigilance & Medical Devices
  DanemarkContacter l’autorité →

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• SUVARNA Ganesh Kumar
  1)The conformity of medical devices is checked in accordance with the QM system (before delivery) (Article 10(9)). 2)The technical documentation is kept up to date (Article 10(4) and (6)). 3) Market surveillance is performed in compliance with the EU regulations (Article 10(10)). 4)The reporting obligations according to the EU regulations are met (Article 10(13)).
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Aucun dispositif enregistré pour ce fabricant.