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Α1-Microglobulin Reagent Kit(latex Enhanced Immunoturbidimetric Method)

EUDAMED

Class IVD General (EU MDR)

Ref 3021679Model R1: 4x50mL, R2: 2x25mL,Calibration sample: 1x1mL, Control: 2x1mL

by Dirui Industrial Co., Ltd

Identity

Trade Name
α1-MICROGLOBULIN REAGENT KIT(LATEX ENHANCED IMMUNOTURBIDIMETRIC METHOD) EUDAMED
Device Name
α1-MICROGLOBULIN REAGENT KIT(LATEX ENHANCED IMMUNOTURBIDIMETRIC METHOD) EUDAMED
Model / Reference
R1: 4x50mL, R2: 2x25mL,Calibration sample: 1x1mL, Control: 2x1mL EUDAMED
3021679 EUDAMED

Identifiers

Primary DI / UDI-DI
06925794592026 EUDAMED
Basic UDI-DI
B-06925794592026 EUDAMED
EMDN Code
W0102019004 A1-MICROGLOBULIN EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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

Α1-Microglobulin Reagent Kit(latex Enhanced Immunoturbidimetric Method) by Dirui Industrial 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-000001891
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 29f45408-4279-4524-882e-0926b1e112b7 61 fields · synced Jun 19, 2026