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α1-Microglobulin Assay Kit (Latex Immunoturbidimetric Method)

EUDAMED

Class IVD General (EU MDR)

Ref DTSH030706Model R1: 90 mL×2; R2: 15 mL×3

by Da Te Bioengineering Technology Co., LTD.

Identity

Device Name
α1-Microglobulin Assay Kit (Latex Immunoturbidimetric Method) EUDAMED
Model / Reference
R1: 90 mL×2; R2: 15 mL×3 EUDAMED
DTSH030706 EUDAMED

Identifiers

Primary DI / UDI-DI
06975225463746 EUDAMED
Basic UDI-DI
B-06975225463746 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 1a86bf8f-977a-4ac7-899b-c9752f244abf 61 fields · synced Jun 19, 2026