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H. Pylori Antigen Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref HP-F02a

by Hangzhou Aichek Medical Technology Co., Ltd.

Identity

Trade Name
H. Pylori Antigen Rapid Test EUDAMED
Device Name
H. Pylori Antigen Rapid Test EUDAMED
Model / Reference
HP-F02a EUDAMED

Identifiers

Primary DI / UDI-DI
D-HP-F02aQX EUDAMED
Basic UDI-DI
B-HP-F02aQX EUDAMED
EMDN Code
W0105090102 H. PYLORI - RT & POC EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Spain 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

H. Pylori Antigen Rapid Test by Hangzhou Aichek Medical Technology 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-000028093
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (1)

  • EUDAMED e52f2b8e-c06b-4625-80e8-cb56158254af 61 fields · synced Jul 8, 2026