EUDAMED last updated this device on Feb 24, 2024
TESSYS® Endo-Flexprobe Handle
B-04250337101192On 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 →- 04250337101192
- Reference / catalog number
- TEFH45025
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.
TESSYS® Endo-Flexprobe Handle 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.