EUDAMED last updated this device on Jul 14, 2026
2101080
8718868776C-3POR2D2NG- Applicable legislation
- —
- Organization name
- NTOC medische techniek 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 →- 08720167718960
- Reference / catalog number
- 2101080
2101080 is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by NTOC medische techniek B.V.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.