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Carcinoembryonic Antigen (eCLIA)

EUDAMED

Class IVD General (EU MDR)

Ref 0320500503Model 100 TModel 50T, 2x50T, 100T, 2x100T

by Shenzhen Lifotronic Technology Co., Ltd.

Identity

Trade Name
Carcinoembryonic Antigen (eCLIA) EUDAMED
Device Name
Carcinoembryonic Antigen (eCLIA) EUDAMED
Model / Reference
100 T EUDAMED
0320500503 EUDAMED
50T, 2x50T, 100T, 2x100T EUDAMED

Identifiers

Primary DI / UDI-DI
06970341685850 EUDAMED
Basic UDI-DI
B-06970341685850 EUDAMED
69703416803205062JH EUDAMED
EMDN Code
W0102030112 CARCINOEMBRYONIC 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

Carcinoembryonic Antigen (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 1e9e3c80-60de-47a3-b91f-6c8297c8bef4 61 fields · synced Jul 11, 2026
  • EUDAMED 0a4acf90-d664-4f38-8c88-b55f00120d2e 61 fields · synced May 17, 2026