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KaiBiLi COVID-19 Antigen Pro

EUDAMED

Class IVD General (EU MDR)

Ref P211138-5

by Hangzhou Genesis Biodetection and Biocontrol Co., Ltd.

Identity

Trade Name
KaiBiLi COVID-19 Antigen Pro EUDAMED
Device Name
KaiBiLi COVID-19 Antigen Pro EUDAMED
Model / Reference
P211138-5 EUDAMED

Identifiers

Primary DI / UDI-DI
16972698601191 EUDAMED
Basic UDI-DI
B-16972698601191 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

KaiBiLi COVID-19 Antigen Pro 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 eee5bc7e-f69f-4e22-a785-67df705f2822 61 fields · synced Jun 18, 2026