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Hemolytic Agent

EUDAMED

Class A (EU MDR)

Ref XQ-0108-02Model HA-1

by Shenzhen Dymind Biotechnology Co., Ltd.

Identity

Trade Name
Hemolytic Agent EUDAMED
Device Name
Hemolytic Agent EUDAMED
Model / Reference
HA-1 EUDAMED
XQ-0108-02 EUDAMED

Identifiers

Primary DI / UDI-DI
06941377305784 EUDAMED
Basic UDI-DI
697049309W01030000026A8 EUDAMED
Direct Marketing DI
06941377305784 EUDAMED
EMDN Code
W0103010299 OTHER HAEMOGLOBIN (TYPES) TESTING - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Hemolytic Agent by Shenzhen Dymind Biotechnology Co., Ltd. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000024842
Authorised Representative
Eunitor GmbH DE-AR-000005081

Sources (1)

  • EUDAMED b310c707-545c-4f22-a8ad-dd18b35f215b 61 fields · synced Jun 14, 2026