Comply with legislation in Healthcare

As an accredited party, we can help manufacturers and healthcare providers with our standards to comply with various (inter)national legislation and agreements.

This concerns agreements unique coding (ADC), the Dutch Implant Registry (LIR) and the Medical Device Regulation (MDR).

voldoen_aan_wetgeving met GS1 standaarden

Dutch Implant Registry (LIR)

Care institutions must register medical devices in the Dutch Implant Registry (LIR).

Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR)

When you work within the Netherlands (and EU) using medical devices, you should comply with the MDR and and the requirement to identify products