In the field of medical technology products, quality regulations are particularly strict. This applies to all processes, including the means of production used and their environment. Cendres+Métaux has in-depth knowledge of the applicable regulations. Our processing systems and equipment have all the necessary qualifications, including cleaning technology for cleanliness from level 1 (free from operating residues) up to level 4 (with micro - biological requirements) and for clean rooms (ISO class 7). We are regularly certified (MDD 93/42/EEC, ISO 13485 / 14001 / 9001) as well as registered as a subcontractor with the FDA and jPAL. Furthermore, additional customer-specific procedures can also be agreed and integrated.