EUDAMED last updated this device on May 25, 2026
Paranit Šampūns +Kemme
5400951PARSHAMPACZF- Applicable legislation
- —
- Organization name
- Omega Pharma International NV
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 →- 05400951005010
- Reference / catalog number
- CT29975
Paranit Šampūns +Kemme is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Omega Pharma International NV. Placed on the EU market in Latvia. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.