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Glu/Ket/PH/Blood/Pro/Bili/Urobil Test

EUDAMED

Class IVD General (EU MDR)

Ref U02-007

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

Identity

Device Name
Glu/Ket/PH/Blood/Pro/Bili/Urobil Test EUDAMED
Model / Reference
U02-007 EUDAMED

Identifiers

Primary DI / UDI-DI
06941571802065 EUDAMED
Basic UDI-DI
B-06941571802065 EUDAMED
EMDN Code
W0101060204 URINE MULTI-CONSTITUENT TEST STRIPS (MANUAL) 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

Glu/Ket/PH/Blood/Pro/Bili/Urobil 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 f71d0777-639a-4731-a35e-f55a722213a1 61 fields · synced Jun 18, 2026