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Multiple Rapid Real-Time PCR kit for Detection of A E gene and Omicron mutation…

EUDAMED

Class IVD General (EU MDR)

Ref 48Tests/kit

by Beijing Kewei Clinical Diagnostic Reagent Inc

Identity

Device Name
Multiple Rapid Real-Time PCR kit for Detection of A E gene and Omicron mutation of SARS-CoV-2 EUDAMED
Model / Reference
48Tests/kit EUDAMED

Identifiers

Primary DI / UDI-DI
06970664752406 EUDAMED
Basic UDI-DI
B-06970664752406 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

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Multiple Rapid Real-Time PCR kit for Detection of A E gene and Omicron mutation… by Beijing Kewei Clinical Diagnostic Reagent Inc — Class IVD General — IVDD…

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000019125
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED a98a317b-6d18-48e3-996f-7f37a62f5831 61 fields · synced Jul 14, 2026