EUDAMED last updated this device on Sep 7, 2026
Peha -instrument
40495004146KR- Applicable legislation
- —
- Organization name
- PAUL HARTMANN AG
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 →- 04052199761435
- Reference / catalog number
- 991019
Peha -instrument is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by PAUL HARTMANN AG. Placed on the EU market in Czechia. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.