Officers and regulatory representatives of FARTO S.R.L. - FARMACO BIOCHIMICO TOSCANO
PARLATI Angela
check the conformity of the device based on the quality management system under which the devices are manufactured, before a device is released; draw up, keep up-to-date the technical documentation and the EU declaration of conformity;ensure the post-market surveillance obligations in accordance with Article 10(10);ensure the reporting obligations referred to in Articles 87 to 91; in the case of investigational devices, issue the statement referred to in Section 4.1 of Chapter II of Annex XV
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Device catalog for FARTO S.R.L. - FARMACO BIOCHIMICO TOSCANO
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Certificate health for FARTO S.R.L. - FARMACO BIOCHIMICO TOSCANO
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Statistics for FARTO S.R.L. - FARMACO BIOCHIMICO TOSCANO