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Cowingene Dengue Virus I/II/III/IV Detection Kit

EUDAMED

Class IVD General (EU MDR)

Ref FE02021X, FE02022X, FE02023W

by Taizhou Cowingene Biotech Co., Ltd.

Identity

Trade Name
Cowingene Dengue Virus I/II/III/IV Detection Kit EUDAMED
Device Name
Cowingene Dengue Virus I/II/III/IV Detection Kit EUDAMED
Model / Reference
FE02021X, FE02022X, FE02023W EUDAMED

Identifiers

Primary DI / UDI-DI
D-FE02GS EUDAMED
Basic UDI-DI
B-FE02GS EUDAMED
EMDN Code
W0105040511 DENGUE VIRUS - NA REAGENTS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

Yes

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

Cowingene Dengue Virus I/II/III/IV Detection Kit by Taizhou Cowingene Biotech 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-000042619
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (2)

  • EUDAMED 73c3beed-0305-457e-965b-39f990005478 61 fields · synced Jul 14, 2026
  • EUDAMED 73c3beed-0305-457e-965b-39f990005478-1 61 fields · synced Jun 10, 2026