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α1-Microglobulin Assay Kit (Latex Immunoturbidimetric Method)

EUDAMED

Class IVD General (EU MDR)

Ref DTSH030705CModel R1: 80 mL×3; R2: 20 mL×3; Calibrator: 1 mL × 1; quality control: 1 mL × 1

by Da Te Bioengineering Technology Co., LTD.

Identity

Device Name
α1-Microglobulin Assay Kit (Latex Immunoturbidimetric Method) EUDAMED
Model / Reference
R1: 80 mL×3; R2: 20 mL×3; Calibrator: 1 mL × 1; quality control: 1 mL × 1 EUDAMED
DTSH030705C EUDAMED

Identifiers

Primary DI / UDI-DI
06975225463739 EUDAMED
Basic UDI-DI
B-06975225463739 EUDAMED
EMDN Code
W0102010405 LIPOPROTEIN ( A ) EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

Yes

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

Category: Apolipoprotein B (Apo B) IVD, reagent

α1-Microglobulin Assay Kit (Latex Immunoturbidimetric Method) by Da Te Bioengineering Technology Co., LTD. — Class IVD General — IVDD — listed in EUDAMED

Similar devices

Also classified as Apolipoprotein B (Apo B) IVD, reagent.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000028832
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 46e3dbc3-3f24-45b5-8064-6858bf6d2c6d 61 fields · synced Jun 18, 2026