Besluit van 4 november 2008, houdende wijziging van het Besluit actieve implantaten en het Besluit medische hulpmiddelen

This legislative decision updates existing Dutch regulations regarding active implants and medical devices. It aims to align national legal frameworks with broader standards to ensure the safety and efficacy of medical technologies used in healthcare. The changes affect manufacturers, distributors, and healthcare providers operating in the Netherlands. These entities must comply with the updated rules when placing active implants and other medical devices on the market.