Officers and regulatory representatives of AngioDynamics Netherlands BV
JORDAN Simon
From an Authorized Representative perspective: (a) the conformity of the devices is appropriately checked before a device is released; (b) the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; (c) the post-market surveillance obligations are complied with in accordance with in accordance with Article 10(10) (d) the reporting obligations referred to in Articles 87 to 91 are fulfilled;
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Device catalog for AngioDynamics Netherlands BV
No devices registered for this manufacturer.
Certificate health for AngioDynamics Netherlands BV