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Alkaline Phosphatase Reagent Kit(ifcc Method)

EUDAMED

Class IVD General (EU MDR)

Ref 3016537Model R1: 4x50mL, R2: 2x25mL

by Dirui Industrial Co., Ltd

Identity

Trade Name
ALKALINE PHOSPHATASE REAGENT KIT(IFCC METHOD) EUDAMED
Device Name
ALKALINE PHOSPHATASE REAGENT KIT(IFCC METHOD) EUDAMED
Model / Reference
R1: 4x50mL, R2: 2x25mL EUDAMED
3016537 EUDAMED

Identifiers

Primary DI / UDI-DI
06942202258916 EUDAMED
Basic UDI-DI
B-06942202258916 EUDAMED
EMDN Code
W01010105 ALKALINE PHOSPHATASE - TOTAL EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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

Alkaline Phosphatase Reagent Kit(ifcc Method) by Dirui Industrial 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-000001891
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 8a1026e5-fe6e-46ee-9b96-63b9c2572546 61 fields · synced Jun 18, 2026