Officers and regulatory representatives of Triangle Surgical Europe OÜ
HAY Andrew
(a)conformity of the devices is appropriately checked, in accordance with the QMS under which the devices are manufactured, before a device is released; (b)technical documentation and the EU DoC are drawn up and kept up-to-date; (c)PMS obligations are complied with in accordance with Article 10(9); (d) the reporting obligations referred to in Articles 82 to 86 are fulfilled; This refers to Vigilance reporting, i.e. serious incident, field safety corrective action, and incident trend reporting).
Hidden
Device catalog for Triangle Surgical Europe OÜ
No devices registered for this manufacturer.
Certificate health for Triangle Surgical Europe OÜ