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Cowingene HPV (2+12) Detection Kit

EUDAMED

Class IVD General (EU MDR)

Ref HP02021X, HP02022X, HP02023W

by Taizhou Cowingene Biotech Co., Ltd.

Identity

Trade Name
Cowingene HPV (2+12) Detection Kit EUDAMED
Device Name
Cowingene HPV (2+12) Detection Kit EUDAMED
Model / Reference
HP02021X, HP02022X, HP02023W EUDAMED

Identifiers

Primary DI / UDI-DI
D-HP02JX EUDAMED
Basic UDI-DI
B-HP02JX EUDAMED
EMDN Code
W0105041002 SCREENING HIGH-RISK HPV - 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 HPV (2+12) Detection Kit by Taizhou Cowingene Biotech Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

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 1e219589-7026-4d89-b1ab-55b62473396a 61 fields · synced Jun 18, 2026
  • EUDAMED 1e219589-7026-4d89-b1ab-55b62473396a-1 61 fields · synced Jun 10, 2026