← Back to catalogue

Dirui

EUDAMED

Class IVD General (EU MDR)

Ref 3011407Model R1:1x20ml, R2:1x5ml, R3:1x30ml, Glycated albumin control: 2x1mL

by Dirui Industrial Co., Ltd

Identity

Trade Name
DIRUI EUDAMED
Device Name
Glycated Albumin Reagent Kit (Ketamine Oxidase Assay) EUDAMED
Model / Reference
R1:1x20ml, R2:1x5ml, R3:1x30ml, Glycated albumin control: 2x1mL EUDAMED
3011407 EUDAMED

Identifiers

Primary DI / UDI-DI
06942202238413 EUDAMED
Basic UDI-DI
B-06942202238413 EUDAMED
EMDN Code
W0102019099 SPECIFIC PROTEINS - OTHER 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

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

Dirui 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000001891
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 6ff2a2a3-5ab3-44f5-a9ab-ff3f6cfef43e 61 fields · synced May 23, 2026