MDR - Important information and recommendations regarding the European Medical Device Regulation
VITA Zahnfabrik H. Rauter · #103201 · source
Information and recommendations regarding the European Medical Device Regulation (MDR), including guidance on Unique Device Identification (UDI) systems, UDI-compliant Health International Bar Code (HIBC) labeling, batch traceability requirements for VITA veneering materials, CAD/CAM materials, and prosthetic teeth, and documentation procedures for medical device compliance.
Informations produit
| Fabricant | VITA Zahnfabrik H. Rauter |
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