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Dus R-600s

EUDAMED

Class A (EU MDR)

Ref 5360Model CYBOW R-600S

by DFI Co., Ltd.

Identity

Trade Name
DUS R-600S EUDAMED
Device Name
CYBOW R-600S EUDAMED
Model / Reference
CYBOW R-600S EUDAMED
5360 EUDAMED

Identifiers

Primary DI / UDI-DI
08806141302735 EUDAMED
Basic UDI-DI
88061413UR6100GV EUDAMED
Direct Marketing DI
08806141302735 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-600s 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 585b3b46-71c5-4685-afe7-c4a888a1fc33 61 fields · synced Jun 18, 2026