udi_ivdLeafLevel 2
UDI for IVDs
The entry udi_ivd denotes the requirement for a Unique Device Identifier on in-vitro diagnostic medical devices under the EU In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746, aimed at ensuring traceability, safety and effective market surveillance throughout the product's lifecycle.
GET
/api/v1/systems/reg_ivdr/nodes/udi_ivdCross-system equivalences0
No cross-system equivalences mapped for this node.