EUDAMED last updated this device on Aug 17, 2026
TT-12580
B-08717903349052On the marketClass III
- Applicable legislation
- —
- Organization name
- CuraMedical B.V.
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 →- 08717903349052
- Reference / catalog number
- TT-12580
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.
TT-12580 is an EU-regulated medical device registered in EUDAMED. It is classified as Class III. Manufactured by CuraMedical B.V.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.