Dirigeants et représentants réglementaires de Mozarc Medical Ireland Ltd.
LANCINI Barbara
Ensure:
the technical documentation and declaration of conformity with a proper conformity assessment pathway are drawn up, kept up to date and available in English in case of HPRA request.
the authorised representative/PRRC are registered in Eudamed and manufacturer has registered its devices in Eudamed
cooperation with HPRA to reduce device risks and provide device samples immediate information is provided to the manufacturer in case of complaints termination of the mandate for due causes
Masqué
Catalogue des dispositifs de Mozarc Medical Ireland Ltd.
Aucun dispositif enregistré pour ce fabricant.
Santé des certificats de Mozarc Medical Ireland Ltd.