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koumd

EUDAMED

Class A (EU MDR)

Ref No additive TubeModel No additive Tube/Clot Activator Tube/Clot Activator With GelTube/Lithium Heparin With GelHeparin Tube/Glucose Tube/EDTA With Gel Tube/EDTA Tube/Coagulation Tube/ESR Tube

by Yiwu Eason Medical Devices Co., Ltd.

Identity

Trade Name
koumd EUDAMED
Device Name
Vacuum Blood Collection Tube EUDAMED
Model / Reference
No additive Tube/Clot Activator Tube/Clot Activator With GelTube/Lithium Heparin With GelHeparin Tube/Glucose Tube/EDTA With Gel Tube/EDTA Tube/Coagulation Tube/ESR Tube EUDAMED
No additive Tube EUDAMED

Identifiers

Primary DI / UDI-DI
06977346240824 EUDAMED
Basic UDI-DI
697734624VBCT01SB EUDAMED
EMDN Code
W050101010201,W050101010202 EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

koumd by Yiwu Eason Medical Devices Co., Ltd. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000041286
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED d33fa370-fc00-42bb-8e91-67a13b2dc8df 61 fields · synced Jun 18, 2026