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Diagnostic Kit for T3 (Time-resolved Fluorescence Immunochromatographic Assay)

EUDAMED

Class IVD General (EU MDR)

Ref SUPF022025

by Shenzhen Superbio Technology Co., Ltd.

Identity

Trade Name
Diagnostic Kit for T3 (Time-resolved Fluorescence Immunochromatographic Assay) EUDAMED
Device Name
Diagnostic Kit for T3 (Time-resolved Fluorescence Immunochromatographic Assay) EUDAMED
Model / Reference
SUPF022025 EUDAMED

Identifiers

Primary DI / UDI-DI
06974521000747 EUDAMED
Basic UDI-DI
B-06974521000747 EUDAMED
EMDN Code
W01020405 TRIIODOTHYRONINE EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Ireland 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

Diagnostic Kit for T3 (Time-resolved Fluorescence Immunochromatographic Assay) by Shenzhen Superbio Technology Co., Ltd. — Class IVD General — IVDD — listed…

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000024149
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED f3bd6caf-c9ad-45a6-94e7-b65f4793177b 61 fields · synced Jun 18, 2026