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5’-Nucleotidase Assay Kit (Peroxidase Method)

EUDAMED

Class IVD General (EU MDR)

Ref DTSH021003CModel R1: 50 mL×1; R2: 25 mL×1; Calibrator: 1 mL × 1; quality control: 1 mL × 1

by Da Te Bioengineering Technology Co., LTD.

Identity

Device Name
5’-Nucleotidase Assay Kit (Peroxidase Method) EUDAMED
Model / Reference
R1: 50 mL×1; R2: 25 mL×1; Calibrator: 1 mL × 1; quality control: 1 mL × 1 EUDAMED
DTSH021003C EUDAMED

Identifiers

Primary DI / UDI-DI
06975225464033 EUDAMED
Basic UDI-DI
B-06975225464033 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

5’-Nucleotidase Assay Kit (Peroxidase 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 925bca2b-3838-43cb-a317-9d8802449c51 61 fields · synced Jun 17, 2026