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Lupus Anticoagulant Assay Kit (Coagulation Method)

EUDAMED

Class IVD General (EU MDR)

Ref NX-0034-07Model CA LA-dRVVT Specification 4 dRVVT confirm: 1 x 2.0 mL

by Shenzhen Dymind Biotechnology Co., Ltd.

Identity

Trade Name
Lupus Anticoagulant Assay Kit (Coagulation Method) EUDAMED
Device Name
Lupus Anticoagulant Assay Kit (Coagulation Method) EUDAMED
Model / Reference
CA LA-dRVVT Specification 4 dRVVT confirm: 1 x 2.0 mL EUDAMED
NX-0034-07 EUDAMED

Identifiers

Primary DI / UDI-DI
06941377305968 EUDAMED
Basic UDI-DI
B-06941377305968 EUDAMED
EMDN Code
W0103020606 LUPUS ANTICOAGULANT EUDAMED

Classification

Device Class
Class IVD General 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

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Lupus Anticoagulant Assay Kit (Coagulation 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 767c2ea6-96db-450b-a239-9e6727118582 61 fields · synced Jun 18, 2026