EUDAMED last updated this device on Jul 14, 2026
220501502
8718868776C-3POR2D2NGOn the marketClass I
- 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 →- 08720167726880
- Reference / catalog number
- 220501502
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.
220501502 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.