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HCV Hepatitis C Virus Rapid Test Device (Serum/Plasma)

EUDAMED

Class IVD Annex II List A (EU MDR)

Ref IHC-302

by Abon Biopharm(Hangzhou) Co., Ltd

Identity

Device Name
HCV Hepatitis C Virus Rapid Test Device (Serum/Plasma) EUDAMED
Model / Reference
IHC-302 EUDAMED

Identifiers

Primary DI / UDI-DI
06952999407510 EUDAMED
Basic UDI-DI
B-06952999407510 EUDAMED
EMDN Code
W0105090202 HCV ANTIBODY -RT & POC EUDAMED

Classification

Device Class
Class IVD Annex II List A EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

HCV Hepatitis C Virus Rapid Test Device (Serum/Plasma) by Abon Biopharm(Hangzhou) Co., Ltd — Class IVD Annex II List A — 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-000009171
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (1)

  • EUDAMED 61fa7cf1-7984-4681-815c-170263071dc0 61 fields · synced Jun 18, 2026