Besluit van 22 juli 2002, houdende wijziging van het besluit medische hulpmiddelen in verband met derivaten van menselijk bloed ref: Staatsblad n° 437 du 22/08/2002

This decision amends existing regulations concerning medical devices, specifically focusing on products derived from human blood. It ensures that these sensitive medical products meet required safety and quality standards. The changes affect manufacturers and distributors of blood-derived medical devices, as well as healthcare providers and patients who use these products. It aims to enhance patient safety and product efficacy.