EUDAMED last updated this device on Sep 26, 2026
KLS Martin
40576051134WOn the marketClass IIb
- Applicable legislation
- —
- Organization name
- KLS Martin SE & Co. KG
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 →- 04057605462371
- Reference / catalog number
- 50-347-09-09
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.
KLS Martin is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by KLS Martin SE & Co. KG. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.