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Squamous Cell Carcinoma (eCLIA)

EUDAMED

Class IVD General (EU MDR)

Ref 0320501202Model 2×50TRef 0320501202 2Model 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
2×50T EUDAMED
0320501202 EUDAMED
50T, 2x50T, 100T, 2x50T EUDAMED
0320501202 2 EUDAMED

Identifiers

Primary DI / UDI-DI
06975984063553 EUDAMED
Basic UDI-DI
B-06975984063553 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 0cc17b30-7854-4567-bbc6-06edc5736e99 61 fields · synced Jun 20, 2026
  • EUDAMED fb62b7f2-e0c1-4623-bdda-447aa7d4c06f 61 fields · synced May 18, 2026