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Myoglobin Reagent Kit(latex Enhanced Immunoturbidimetric Method)

EUDAMED

Class IVD General (EU MDR)

Ref 3016165Model R1: 2x60mL, R2: 2x20mL, Calibration sample: 5x0.5mL, Control: 2x0.5mL

by Dirui Industrial Co., Ltd

Identity

Trade Name
MYOGLOBIN REAGENT KIT(LATEX ENHANCED IMMUNOTURBIDIMETRIC METHOD) EUDAMED
Device Name
MYOGLOBIN REAGENT KIT(LATEX ENHANCED IMMUNOTURBIDIMETRIC METHOD) EUDAMED
Model / Reference
R1: 2x60mL, R2: 2x20mL, Calibration sample: 5x0.5mL, Control: 2x0.5mL EUDAMED
3016165 EUDAMED

Identifiers

Primary DI / UDI-DI
06942202246982 EUDAMED
Basic UDI-DI
B-06942202246982 EUDAMED
EMDN Code
W01021304 MYOGLOBIN EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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

Myoglobin Reagent Kit(latex Enhanced Immunoturbidimetric Method) by Dirui Industrial Co., Ltd — Class IVD General — IVDD — listed in EUDAMED

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 aefe1211-1acc-4a49-9ff1-3f45fc6c7d7f 61 fields · synced Jun 17, 2026