EUDAMED last updated this device on Aug 19, 2026
Glimessen
697790480G524000000000HAOn the marketClass I
- Applicable legislation
- —
- Organization name
- Hangzhou Hikimaging Electronics Co., Ltd.
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 →- 06977904801009
- Reference / catalog number
- P524V
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.
Glimessen is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Hangzhou Hikimaging Electronics Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.