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ANTICHEK SARS-CoV-2 (COVID-19) Antigen Test

EUDAMED

Class IVD General (EU MDR)

Ref P211135

by Hangzhou Genesis Biodetection and Biocontrol Co., Ltd.

Identity

Trade Name
ANTICHEK SARS-CoV-2 (COVID-19) Antigen Test EUDAMED
Device Name
ANTICHEK SARS-CoV-2 (COVID-19) Antigen Test EUDAMED
Model / Reference
P211135 EUDAMED

Identifiers

Primary DI / UDI-DI
16972698601184 EUDAMED
Basic UDI-DI
B-16972698601184 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

ANTICHEK SARS-CoV-2 (COVID-19) Antigen 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 e1c88ef8-2bb9-4bc0-8e47-e8c17c87d19a 61 fields · synced Jun 20, 2026