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H.pylori Antigen Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref P221007

by Hangzhou Genesis Biodetection and Biocontrol Co., Ltd.

Identity

Trade Name
H.pylori Antigen Rapid Test EUDAMED
Device Name
H.pylori Antigen Rapid Test EUDAMED
Model / Reference
P221007 EUDAMED

Identifiers

Primary DI / UDI-DI
16972698600194 EUDAMED
Basic UDI-DI
B-16972698600194 EUDAMED
EMDN Code
W0105099099 VIROLOGY - RT & POC - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Netherlands 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 Genesis Biodetection and Biocontrol Co., Ltd. — Class IVD General — 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-000013495
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 670a163f-418e-460f-a4fa-66f6c12fac6e 61 fields · synced Jun 18, 2026