EUDAMED last updated this device on Jul 15, 2026
IKAZUCHI Zero
B-04540778150201On the marketClass III
- Applicable legislation
- —
- Organization name
- KANEKA 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 →- 04540778150201
- Reference / catalog number
- ZE-18-150
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.
IKAZUCHI Zero is an EU-regulated medical device registered in EUDAMED. It is classified as Class III. Manufactured by KANEKA Corporation. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.