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Rapid Influenza A+B Antigen Test Card

EUDAMED

Class IVD General (EU MDR)

Ref 1N18C5

by Xiamen Boson Biotech Co., Ltd.

Identity

Trade Name
Rapid Influenza A+B Antigen Test Card EUDAMED
Device Name
Rapid Influenza A+B Antigen Test Card EUDAMED
Model / Reference
1N18C5 EUDAMED

Identifiers

Primary DI / UDI-DI
06921963710895 EUDAMED
Basic UDI-DI
B-06921963710895 EUDAMED
EMDN Code
W0105099004 INFLUENZA A AND /OR B - RT & POC EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany 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

Rapid Influenza A+B Antigen Test Card by Xiamen Boson Biotech 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-000001096
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 4d288bb0-39ad-402a-845d-f7027ce5ae42 61 fields · synced Jul 24, 2026