Key facts
- Aphranel MagiCCrystal CaHA Filler received EU MDR certification on May 18, 2026.
- The certification allows the product to be marketed in the European Union.
- Moyom Biotechnology is the manufacturer of the filler.
The European Union's Medical Device Regulation (EU MDR) is a stringent set of rules governing the safety and performance of medical devices sold within the EU. Obtaining this certification is a significant step for medical aesthetic products, indicating compliance with high standards for quality and patient safety. This allows Moyom Biotechnology to expand its market reach into the European Union.