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Dus R-300

EUDAMED

Class A (EU MDR)

Ref 5260Model CYBOW Reader 300

by DFI Co., Ltd.

Identity

Trade Name
DUS R-300 EUDAMED
Device Name
CYBOW Reader 300 EUDAMED
Model / Reference
CYBOW Reader 300 EUDAMED
5260 EUDAMED

Identifiers

Primary DI / UDI-DI
08806141302155 EUDAMED
Basic UDI-DI
88061413UR6200H2 EUDAMED
EMDN Code
W02010701 URINALYSIS (UR) - LABORATORY ANALYSERS- INSTRUMENTS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany 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

Yes

EUDAMED

New Device

No

EUDAMED

Dus R-300 by DFI 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

Manufacturer
DFI Co., Ltd.
EUDAMED SRN
KR-MF-000015786
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 6b816c25-2dfe-40b8-99a8-f94c6adcaaa0 61 fields · synced Jul 16, 2026