← Back to catalogue

Squamous Cell Carcinoma (eCLIA)

EUDAMED

Class C (EU MDR)

Ref 0320501203Model 50T, 2x50T, 100T, 2x50TModel 100T

by Shenzhen Lifotronic Technology Co., Ltd.

Identity

Trade Name
Squamous Cell Carcinoma (eCLIA) EUDAMED
Device Name
Squamous Cell Carcinoma (eCLIA) EUDAMED
Model / Reference
50T, 2x50T, 100T, 2x50T EUDAMED
0320501203 EUDAMED
100T EUDAMED

Identifiers

Primary DI / UDI-DI
06970341689230 EUDAMED
Basic UDI-DI
69703416803205050JA EUDAMED
B-06970341689230 EUDAMED
EMDN Code
W0102030116 SQUAMOUS CELL CARCINOMA ANTIGEN EUDAMED

Classification

Device Class
Class C EUDAMED
Class IVD General 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 C — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED 0ab6164e-ac59-46a6-82a8-a6f3f8e8b45c 61 fields · synced Aug 1, 2026
  • EUDAMED d953452e-d451-4e04-b282-97ebcf07988b 61 fields · synced May 17, 2026