← Back to catalogue

Hepatitis A Virus Rapid Test - Serum

EUDAMED

Class IVD General (EU MDR)

Ref HAV-4012/HAV-4022/HAV-3012/HAV-3022

by Safecare Biotech (hangzhou) Co., Ltd.

Identity

Trade Name
Hepatitis A Virus Rapid Test (Whole Blood/Serum/Plasma) EUDAMED
Device Name
Hepatitis A Virus Rapid Test (Whole Blood/Serum/Plasma) EUDAMED
Model / Reference
HAV-4012/HAV-4022/HAV-3012/HAV-3022 EUDAMED

Identifiers

Primary DI / UDI-DI
D-697424646HAV000GQVC EUDAMED
Basic UDI-DI
B-697424646HAV000GQVC EUDAMED
EMDN Code
W0105090299 HEPATITIS VIRUSES - RT & POC - OTHER EUDAMED
Models / Variants
Whole Blood EUDAMED
Serum EUDAMED
Plasma 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

Hepatitis A Virus Rapid Test - Serum by Safecare Biotech (Hangzhou) Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — 3 models

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000019109
Authorised Representative
Wellkang Ltd XI-AR-000001836

Sources (1)

  • EUDAMED 54f79d6a-59fe-4630-b169-5be287f48b03 61 fields · synced Oct 6, 2026