EUDAMED last updated this device on Sep 7, 2026

Peha -instrument

40495004146KR
On the marketClass IIa
Applicable legislation
Organization name
PAUL HARTMANN AG
04052199761435
Reference / catalog number
991019
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.

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.