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TT3 Test Kit (Dry Fluorescence Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref 0003-03

by Lansion Biotechnology Co., Ltd.

Identity

Device Name
TT3 Test Kit (Dry Fluorescence Immunoassay) EUDAMED
Model / Reference
0003-03 EUDAMED

Identifiers

Primary DI / UDI-DI
06971763220032 EUDAMED
Basic UDI-DI
B-06971763220032 EUDAMED
EMDN Code
W01020405 TRIIODOTHYRONINE 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

TT3 Test Kit (Dry Fluorescence Immunoassay) by Lansion 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-000001086
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 3ac14b5f-06cd-4343-8b47-84f4a0964013 61 fields · synced Jul 28, 2026