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High-Level Feritin Whole Blood/Serum Test

EUDAMED

Class IVD General (EU MDR)

Ref R101-116

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

Identity

Device Name
High-Level Feritin Whole Blood/Serum Test EUDAMED
Model / Reference
R101-116 EUDAMED

Identifiers

Primary DI / UDI-DI
06941571810145 EUDAMED
Basic UDI-DI
B-06941571810145 EUDAMED
EMDN Code
W01021699 RAPID TESTS & POINT OF CARE - IMMUNOCHEMISTRY - 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

Yes

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

High-Level Feritin Whole Blood/Serum Test by Ameritech Diagnostic Reagent (Jiaxing) Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

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 (1)

  • EUDAMED 98a36cc7-f857-4ad3-8243-81edf06faedf 61 fields · synced Jun 19, 2026