EUDAMED last updated this device on Jul 7, 2026
850 MiYO TRANS CLEMENTINE fluor.
42520058001H8On the marketClass IIa
- Applicable legislation
- —
- Organization name
- Chemichl AG
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →- 04252005800642
- Reference / catalog number
- 0969
Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.
850 MiYO TRANS CLEMENTINE fluor. is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Chemichl AG. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.