Officers and regulatory representatives of Theras Lifetech S.r.l. Unipersonale
ZANCOLA Silvia
- the conformity of the devices, according to the QMS under which the devices are manufactured, before the device release;
- the technical documentation and the EU declaration of conformity
- the post-market surveillance obligations in accordance with Article 10(10);
- the reporting obligations referred to in Articles 87 to 91;
- in the case of investigational devices, for the statement referred to in Section 4.1 of Chapter II of Annex XV.
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Device catalog for Theras Lifetech S.r.l. Unipersonale
No devices registered for this manufacturer.
Certificate health for Theras Lifetech S.r.l. Unipersonale
No certificates registered for this manufacturer.
Statistics for Theras Lifetech S.r.l. Unipersonale