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Anti-Streptolysin O Kit(latex Enhanced Immunoturbidimetric Assay)

EUDAMED

Class IVD General (EU MDR)

Ref 3023200Model R1: 1x40mL, R2: 1x10mL, Calibration sample: 1x1mL,

by Dirui Industrial Co., Ltd

Identity

Trade Name
ANTI-STREPTOLYSIN O KIT(LATEX ENHANCED IMMUNOTURBIDIMETRIC ASSAY) EUDAMED
Device Name
ANTI-STREPTOLYSIN O KIT(LATEX ENHANCED IMMUNOTURBIDIMETRIC ASSAY) EUDAMED
Model / Reference
R1: 1x40mL, R2: 1x10mL, Calibration sample: 1x1mL, EUDAMED
3023200 EUDAMED

Identifiers

Primary DI / UDI-DI
06942202212918 EUDAMED
Basic UDI-DI
B-06942202212918 EUDAMED
EMDN Code
W01021104 ANTI-STREPTOLYSIN O (QUANTITATIVE) 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

Anti-Streptolysin O Kit(latex Enhanced Immunoturbidimetric Assay) 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 24960348-b5d5-4db3-a3f7-8480c314a1f0 61 fields · synced Jun 19, 2026