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Mutation of SARS-CoV-2 nucleic acid Detection Kit (Real Time PCR)

EUDAMED

Class IVD General (EU MDR)

Ref 18-02-0129Model 48 Tests/kit

by Shenzhen Zijian Biotechnology Co., Ltd

Identity

Trade Name
Mutation of SARS-CoV-2 nucleic acid Detection Kit (Real Time PCR) EUDAMED
Device Name
Mutation of SARS-CoV-2 nucleic acid Detection Kit (Real Time PCR) EUDAMED
Model / Reference
48 Tests/kit EUDAMED
18-02-0129 EUDAMED

Identifiers

Primary DI / UDI-DI
06974674891858 EUDAMED
Basic UDI-DI
B-06974674891858 EUDAMED
EMDN Code
W0105040599 VIROLOGY - NA REAGENTS - 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

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

Mutation of SARS-CoV-2 nucleic acid Detection Kit (Real Time PCR) by Shenzhen Zijian Biotechnology 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-000022829
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 1a315808-a30a-44ac-a3e8-cf5ba477e69c 61 fields · synced Jul 16, 2026