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GH FIA Kit

EUDAMED

Class IVD General (EU MDR)

Ref 18-02-0076Model 25 Tests/kit

by Shenzhen Zijian Biotechnology Co., Ltd

Identity

Trade Name
GH FIA Kit EUDAMED
Device Name
GH FIA Kit EUDAMED
Model / Reference
25 Tests/kit EUDAMED
18-02-0076 EUDAMED

Identifiers

Primary DI / UDI-DI
06974674892466 EUDAMED
Basic UDI-DI
B-06974674892466 EUDAMED
EMDN Code
W0102060402 HUMAN GROWTH HORMONE 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

GH FIA Kit 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
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 563f713d-b1d6-4adf-b48c-88e5a8be4870 61 fields · synced Oct 6, 2026