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CEA Serum Test

EUDAMED

Class IVD General (EU MDR)

Ref R20-112Ref R20-110

by Ameritech Diagnostic Reagent (Jiaxing) Co., Ltd.

Identity

Device Name
CEA Serum Test EUDAMED
Model / Reference
R20-112 EUDAMED
R20-110 EUDAMED

Identifiers

Primary DI / UDI-DI
06941571820205 EUDAMED
06941571820106 EUDAMED
Basic UDI-DI
B-06941571820205 EUDAMED
B-06941571820106 EUDAMED
EMDN Code
W0102160299 TUMOUR MARKER RT & POC - OTHER EUDAMED

Classification

Device Class
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

CEA Serum Test by Ameritech Diagnostic Reagent (Jiaxing) Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000020607
Authorised Representative
CEpartner4U NL-AR-000000111

Sources (2)

  • EUDAMED b7ed4864-3438-426e-91f2-19902a4d8185 61 fields · synced Jul 15, 2026
  • EUDAMED 76e16181-bbe4-491e-8b53-2530a75df23c 61 fields · synced May 18, 2026