EUDAMED last updated this device on Sep 10, 2026
115019100
6902139QX02068LX- Applicable legislation
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- Organization name
- Double Medical Technology Inc.
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 →- 06942351350356
- Reference / catalog number
- 115019100
115019100 is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Double Medical Technology Inc.. Placed on the EU market in Hungary. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.