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Automatic Coagulation Analyzer

EUDAMED

Class A (EU MDR)

Ref DM9102DC1280Model CA1200

by Shenzhen Dymind Biotechnology Co., Ltd.

Identity

Trade Name
Automatic Coagulation Analyzer EUDAMED
Device Name
Automatic Coagulation Analyzer EUDAMED
Model / Reference
CA1200 EUDAMED
DM9102DC1280 EUDAMED

Identifiers

Primary DI / UDI-DI
06976117451834 EUDAMED
Basic UDI-DI
6970493090802006PE EUDAMED
Direct Marketing DI
06976117451834 EUDAMED
EMDN Code
W0202020102 AUTOMATED COAGULOMETERS 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

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Automatic Coagulation Analyzer 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 5ea8a85f-4c9e-4463-b397-b231ecd424ce 61 fields · synced Jun 18, 2026