EUDAMED last updated this device on Jun 15, 2026
Auto Hematology Analyzer
6970493090608001PL- Applicable legislation
- —
- Organization name
- Shenzhen Dymind Biotechnology 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 →- 06976117452732
- Reference / catalog number
- XQ-0001-02
Auto Hematology Analyzer is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class B. Manufactured by Shenzhen Dymind Biotechnology Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.