Officers and regulatory representatives of Vantive - Gambro Dialysatoren
KIEFERLE Verena
The technical documentation and the EU declaration of conformity are drawn up and kept up-to-date
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BREIBACH Ines
(a) the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released
(b) the post-market surveillance obligations are complied with in accordance with Article 10(10);
(c) the reporting obligations referred to in Articles 87 to 91 are fulfilled;
(d) in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
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Device catalog for Vantive - Gambro Dialysatoren
No devices registered for this manufacturer.
Certificate health for Vantive - Gambro Dialysatoren