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EZER COVID-19 Antigen Rapid Test

EUDAMED

Class IVD devices for self-testing (EU MDR)

Ref P213104

by Hangzhou Genesis Biodetection and Biocontrol Co., Ltd.

Identity

Trade Name
EZER COVID-19 Antigen Rapid Test EUDAMED
Device Name
EZER COVID-19 Antigen Rapid Test EUDAMED
Model / Reference
P213104 EUDAMED

Identifiers

Primary DI / UDI-DI
16972698600514 EUDAMED
Basic UDI-DI
B-16972698600514 EUDAMED
EMDN Code
W0105099099 VIROLOGY - RT & POC - OTHER EUDAMED

Classification

Device Class
Class IVD devices for self-testing 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

Yes

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

EZER COVID-19 Antigen Rapid Test by Hangzhou Genesis Biodetection and Biocontrol Co., Ltd. — Class IVD devices for self-testing — 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 d481dc2c-6ccb-4ee2-8282-62957bc2fb84 61 fields · synced Jun 19, 2026