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Antithrombin III Testing Kit (Chromogenic Substrate Method)

EUDAMED

Class IVD General (EU MDR)

Ref NX-0007-01Model Model : CA AT-III (L) Specification 2: R1: 3.5 mL × 4, R2: 1.0 mL × 4, R3: 5.0 mL × 4

by Shenzhen Dymind Biotechnology Co., Ltd.

Identity

Trade Name
Antithrombin III Testing Kit (Chromogenic Substrate Method) EUDAMED
Device Name
Antithrombin III Testing Kit (Chromogenic Substrate Method) EUDAMED
Model / Reference
Model : CA AT-III (L) Specification 2: R1: 3.5 mL × 4, R2: 1.0 mL × 4, R3: 5.0 mL × 4 EUDAMED
NX-0007-01 EUDAMED

Identifiers

Primary DI / UDI-DI
06976117454422 EUDAMED
Basic UDI-DI
B-06976117454422 EUDAMED
EMDN Code
W0103020602 ANTITHROMBIN EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Antithrombin III Testing Kit (Chromogenic Substrate Method) by Shenzhen Dymind Biotechnology Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

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

Sources (1)

  • EUDAMED b6da8a84-7c0d-4b07-a7b8-3dbd8808e76d 61 fields · synced Jun 19, 2026