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Prueba Rápida Combinada de Antígenos de COVID-19 y Gripe A+B

EUDAMED

Class IVD devices for self-testing (EU MDR)

Ref FCO-6032H

by Safecare Biotech (hangzhou) Co., Ltd.

Identity

Trade Name
Prueba Rápida Combinada de Antígenos de COVID-19 y Gripe A+B EUDAMED
Device Name
Prueba Rápida Combinada de Antígenos de COVID-19 y Gripe A+B EUDAMED
Model / Reference
FCO-6032H EUDAMED

Identifiers

Primary DI / UDI-DI
06974246460918 EUDAMED
Basic UDI-DI
B-06974246460918 EUDAMED
EMDN Code
W0105090601 CORONAVIRUS / INFLUENZA - RT & POC EUDAMED

Classification

Device Class
Class IVD devices for self-testing EUDAMED
Market of Registration
Spain 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

Prueba Rápida Combinada de Antígenos de COVID-19 y Gripe A+B by Safecare Biotech (Hangzhou) Co., Ltd. — Class IVD devices for self-testing — IVDD — listed in…

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000019109
Authorised Representative
Share info GmbH DE-AR-000005132

Sources (1)

  • EUDAMED 5b20b8a8-2fde-45bc-a692-b929ded83d93 61 fields · synced Oct 6, 2026