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Squamous Cell Carcinoma (eCLIA)

EUDAMED

Class IVD General (EU MDR)

Ref 0320501201Model 50TModel 50T, 2x50T, 100T, 2x50T

by Shenzhen Lifotronic Technology Co., Ltd.

Identity

Trade Name
Squamous Cell Carcinoma (eCLIA) EUDAMED
Device Name
Squamous Cell Carcinoma (eCLIA) EUDAMED
Model / Reference
50T EUDAMED
0320501201 EUDAMED
50T, 2x50T, 100T, 2x50T EUDAMED

Identifiers

Primary DI / UDI-DI
06970341689223 EUDAMED
Basic UDI-DI
B-06970341689223 EUDAMED
69703416803205050JA EUDAMED
EMDN Code
W0102030116 SQUAMOUS CELL CARCINOMA ANTIGEN EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Class C EUDAMED
Market of Registration
Germany 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

New Device

No

EUDAMED

Squamous Cell Carcinoma (eCLIA) by Shenzhen Lifotronic Technology Co., Ltd. — Class IVD General — IVDR, IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000005654
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (2)

  • EUDAMED fd67e2e5-629e-419d-81e5-b5c2d941386d 61 fields · synced Jun 18, 2026
  • EUDAMED 10682378-273a-4c0a-8443-c5a71028ceff 61 fields · synced May 19, 2026