EUDAMED last updated this device on Feb 23, 2024
Revision Instrument Inner Part
B-04250337110552On the marketClass I
- Applicable legislation
- —
- Organization name
- Joimax 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 →- 04250337110552
- Reference / catalog number
- JMPS1053R
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.
Revision Instrument Inner Part is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Joimax GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.