EUDAMED last updated this device on Jun 25, 2026
Rektálny vankúš, 938
858500K58338938AFOn the marketClass I
- Applicable legislation
- —
- Organization name
- PROTETIKA, a.s.
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 →- 08585003403192
- Reference / catalog number
- 8585003403192
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.
Rektálny vankúš, 938 is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by PROTETIKA, a.s.. Placed on the EU market in Slovakia. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.