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SARS-CoV-2/Flu A+B/HPIV2/HPIV1+3/RSV/ADV/MP/SP/HMPV Antigen Rapid Test Kit (Imm…

EUDAMED

Class IVD General (EU MDR)

Ref ICA2521Model 20 Tests/kit

by BioTeke Corporation(Wuxi)Co., Ltd

Identity

Device Name
SARS-CoV-2/Flu A+B/HPIV2/HPIV1+3/RSV/ADV/MP/SP/HMPV Antigen Rapid Test Kit (Immunochromatographic Assay) EUDAMED
Model / Reference
20 Tests/kit EUDAMED
ICA2521 EUDAMED

Identifiers

Primary DI / UDI-DI
06974541565578 EUDAMED
Basic UDI-DI
B-06974541565578 EUDAMED
EMDN Code
W0105099099 VIROLOGY - RT & POC - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Austria 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/Flu A+B/HPIV2/HPIV1+3/RSV/ADV/MP/SP/HMPV Antigen Rapid Test Kit (Imm… by Bioteke Corporation (Wuxi) Co., Ltd. — Class IVD General — IVDD — listed…

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000007517
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (1)

  • EUDAMED 25a28fb8-a018-4590-89a5-2a6225ed80a3 61 fields · synced Jun 19, 2026