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Albumin Urine Test

EUDAMED

Class IVD General (EU MDR)

Ref R50-112Ref R50-110

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

Identity

Device Name
Albumin Urine Test EUDAMED
Model / Reference
R50-112 EUDAMED
R50-110 EUDAMED

Identifiers

Primary DI / UDI-DI
06941571850011 EUDAMED
06941571850004 EUDAMED
Basic UDI-DI
B-06941571850011 EUDAMED
B-06941571850004 EUDAMED
EMDN Code
W0102160101 ALBUMIN INCL. UALBUMIN RT & POC 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

EUDAMEDEUDAMED

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

Albumin Urine 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 abe0bc85-d91c-4843-bc10-1d13857c72bd 61 fields · synced Oct 6, 2026
  • EUDAMED 60ac136c-66e6-4870-b9c2-632b9b3627ef 61 fields · synced May 19, 2026