EUDAMED last updated this device on Jun 25, 2026
BALLOON
B-04961333123339On the marketClass I
- Applicable legislation
- —
- Organization name
- HOYA Corporation
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 →- 04961333123339
- Reference / catalog number
- 04961333123339
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.
BALLOON is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by HOYA Corporation . Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.