Vitra International continues to prioritize quality assurance compliance. Our primary manufacturing facility has completed its annual ISO 13485 (Medical Devices QMS) audit with an outstanding score and zero major non-conformances.
This audit monitors raw material sourcing, material trace certifications, forge heating parameters, heat treatment vacuums, and final polishing controls.
This successful evaluation confirms our compliance with EU Medical Device Regulations (MDR), ensuring our CE mark registrations remain active and our global hospital partnerships remain secure.
