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Duplex Real-time PCR Detection Kit for Bordetella Pertussis

EUDAMED

Class IVD General (EU MDR)

Ref A2472-50T

by Beijing Applied Biological Technologies Co., Ltd.

Identity

Device Name
Duplex Real-time PCR Detection Kit for Bordetella Pertussis EUDAMED
Model / Reference
A2472-50T EUDAMED

Identifiers

Primary DI / UDI-DI
06974323012061 EUDAMED
Basic UDI-DI
B-06974323012061 EUDAMED
EMDN Code
W0105011607 BORDETELLA PERTUSSIS / PARAPERTUSSIS - NA REAGENTS 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

Duplex Real-time PCR Detection Kit for Bordetella Pertussis by Beijing Applied Biological Technologies Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000012338
Authorised Representative
Luxus Lebenswelt GmbH DE-AR-000005110

Sources (1)

  • EUDAMED fde4448c-cbd4-4b6e-9ccc-e63679806e80 61 fields · synced Jul 18, 2026