Besluit van 30/03/1995 medische hulpmiddelen, Staatsblad nr 243 van 1995
This legislative act establishes the national regulations for the safety, quality, and performance of medical devices in the Netherlands. It ensures that medical equipment meets specific health standards before being placed on the market to protect patient and user safety. This affects manufacturers, importers, and distributors of medical devices operating within the Netherlands, as well as healthcare providers using these tools.
National vote coverage: Netherlands-only