EUDAMED last updated this device on Jul 10, 2026
HURO PATH® T
88000385CZHUROTVXOn the marketIVDR Class A
- Applicable legislation
- —
- Organization name
- CelltraZone 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 →- 08800038500327
- Reference / catalog number
- ALBCCZ003
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.
HURO PATH® T is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by CelltraZone Co., Ltd. Placed on the EU market in Romania. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.