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α-Amylase Assay Kit (EPS Method)

EUDAMED

Class IVD General (EU MDR)

Ref DTSH070208Model R1: 40 mL×4; R2: 10 mL×4

by Da Te Bioengineering Technology Co., LTD.

Identity

Device Name
α-Amylase Assay Kit (EPS Method) EUDAMED
Model / Reference
R1: 40 mL×4; R2: 10 mL×4 EUDAMED
DTSH070208 EUDAMED

Identifiers

Primary DI / UDI-DI
06975225460684 EUDAMED
Basic UDI-DI
B-06975225460684 EUDAMED
EMDN Code
W01010107 AMYLASE - TOTAL 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

α-Amylase Assay Kit (EPS Method) by Da Te Bioengineering Technology Co., LTD. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

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 b3ca8a15-38ad-44d6-97a5-74fc7b3ce0c3 61 fields · synced Jun 20, 2026