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H.pylori Antigen Rapid Test Kit(Feces)

EUDAMED

Class IVD General (EU MDR)

Ref HPAg-5011/HPAg-5012

by Safecare Biotech (hangzhou) Co., Ltd.

Identity

Trade Name
H.pylori Antigen Rapid Test Kit(Feces) EUDAMED
Device Name
H.pylori Antigen Rapid Test Kit(Feces) EUDAMED
Model / Reference
HPAg-5011/HPAg-5012 EUDAMED

Identifiers

Primary DI / UDI-DI
D-697424646HP(F)000FQ86 EUDAMED
Basic UDI-DI
B-697424646HP(F)000FQ86 EUDAMED
EMDN Code
W0105090102 H. PYLORI - RT & POC 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

H.pylori Antigen Rapid Test Kit(Feces) by Safecare Biotech (Hangzhou) 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-000019109
Authorised Representative
Wellkang Ltd XI-AR-000001836

Sources (1)

  • EUDAMED 4abe736b-5755-40c8-a382-4004dfab7572 61 fields · synced Jun 19, 2026