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Ischemic Modified Albumin Reagent Kit (ACB Assay)

EUDAMED

Class IVD General (EU MDR)

Ref 3011892Model R1: 1x30mL, R2: 1x10mL, Control: 1x1mL

by Dirui Industrial Co., Ltd

Identity

Trade Name
Ischemic Modified Albumin Reagent Kit (ACB Assay) EUDAMED
Device Name
Ischemic Modified Albumin Reagent Kit (ACB Assay) EUDAMED
Model / Reference
R1: 1x30mL, R2: 1x10mL, Control: 1x1mL EUDAMED
3011892 EUDAMED

Identifiers

Primary DI / UDI-DI
06942202260766 EUDAMED
Basic UDI-DI
B-06942202260766 EUDAMED
EMDN Code
W01021399 CARDIAC MARKERS - 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

Yes

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

Ischemic Modified Albumin Reagent Kit (ACB Assay) 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 1c3b783b-b5a0-4c30-9e86-96f1f3c953eb 61 fields · synced Jul 11, 2026