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SARS-CoV-2 Neutralizing Antibody Rapid Test Device

EUDAMED

Class IVD General (EU MDR)

Ref SARS-CoV-2 Neutralizing Antibody Rapid Test Device

by Farmasino Medical Co., Ltd

Identity

Device Name
SARS-CoV-2 Neutralizing Antibody Rapid Test Device EUDAMED
Model / Reference
SARS-CoV-2 Neutralizing Antibody Rapid Test Device EUDAMED

Identifiers

Primary DI / UDI-DI
06975445472054 EUDAMED
Basic UDI-DI
B-06975445472054 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

SARS-CoV-2 Neutralizing Antibody Rapid Test Device by Farmasino Medical 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-000026190
Authorised Representative
Humiss International B.V. NL-AR-000001490

Sources (1)

  • EUDAMED 849193cd-4fb9-4103-a22c-a948bd2ad3aa 61 fields · synced Oct 6, 2026