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i-Check Cartridge

EUDAMED

Class IVD General (EU MDR)

Ref BG3

by B&E Bio-Technology Co., Ltd.

Identity

Device Name
i-Check Cartridge EUDAMED
Model / Reference
BG3 EUDAMED

Identifiers

Primary DI / UDI-DI
16972337852205 EUDAMED
Basic UDI-DI
B-16972337852205 EUDAMED
EMDN Code
W0201040185 BLOOD GAS ANALYSERS - CONSUMABLES 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

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

i-Check Cartridge by B&E Bio-Technology 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-000023256
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED ed1109fe-64c1-45a1-9708-04b05019412a 61 fields · synced Jun 18, 2026