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Carcinoembryonic Antigen (eCLIA)

EUDAMED

Class C (EU MDR)

Ref 0320500502Model 50T, 2x50T, 100T, 2x100TModel 2×50 T

by Shenzhen Lifotronic Technology Co., Ltd.

Identity

Trade Name
Carcinoembryonic Antigen (eCLIA) EUDAMED
Device Name
Carcinoembryonic Antigen (eCLIA) EUDAMED
Model / Reference
50T, 2x50T, 100T, 2x100T EUDAMED
0320500502 EUDAMED
2×50 T EUDAMED

Identifiers

Primary DI / UDI-DI
06975984063430 EUDAMED
Basic UDI-DI
69703416803205062JH EUDAMED
B-06975984063430 EUDAMED
EMDN Code
W0102030112 CARCINOEMBRYONIC 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

Carcinoembryonic Antigen (eCLIA) by Shenzhen Lifotronic Technology Co., Ltd. — Class C — IVDD, IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

European Union Active

CE/IVDR

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Manufacturer

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

Sources (2)

  • EUDAMED 84abc254-fc0f-4c37-b856-ad838d76d120 61 fields · synced Jul 14, 2026
  • EUDAMED 096eb716-d5c9-4ba3-a47c-c76112ff2a6a 61 fields · synced May 19, 2026