EUDAMED last updated this device on Jul 10, 2026
HURO PATH® Filter
88000385CZFSTDNZOn 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 →- 08800038500419
- Reference / catalog number
- AFSTD001
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® Filter 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 Hungary. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.