EUDAMED last updated this device on Jul 15, 2026
ALPHANOVOCAM
4049047ZAE13ACA27CWEQ4- Applicable legislation
- —
- Organization name
- Gimmi GmbH
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 →- 04049047640851
- Reference / catalog number
- S.2002.38
ALPHANOVOCAM is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Gimmi GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.