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COVID-19 Neutralizing Antibody Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref COV-W23001

by Assure Tech. (Hangzhou) Co., Ltd.

Identity

Trade Name
COVID-19 Neutralizing Antibody Rapid Test EUDAMED
Device Name
COVID-19 Neutralizing Antibody Rapid Test EUDAMED
Model / Reference
COV-W23001 EUDAMED

Identifiers

Primary DI / UDI-DI
06952804803148 EUDAMED
Basic UDI-DI
B-06952804803148 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

No

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

COVID-19 Neutralizing Antibody Rapid Test by Assure Tech. (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-000002170
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 9a10333e-70b4-477a-9134-c9d40992d6ce 61 fields · synced Jul 19, 2026