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Testosterone(T)Detection Kit(CLIA)

EUDAMED

Class IVD General (EU MDR)

Ref 18-02-0155Model 50 Tests/kit

by Shenzhen Zijian Biotechnology Co., Ltd

Identity

Trade Name
Testosterone(T)Detection Kit(CLIA) EUDAMED
Device Name
Testosterone(T)Detection Kit(CLIA) EUDAMED
Model / Reference
50 Tests/kit EUDAMED
18-02-0155 EUDAMED

Identifiers

Primary DI / UDI-DI
06974674892831 EUDAMED
Basic UDI-DI
B-06974674892831 EUDAMED
EMDN Code
W0102050110 TESTOSTERONE (WITH DEHYDRO AND FREE TESTOSTERONE) 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

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Testosterone(T)Detection Kit(CLIA) by Shenzhen Zijian Biotechnology 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-000022829
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 5c323dc2-2168-4ccf-b576-532d0314a0ef 61 fields · synced Jul 8, 2026