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Cybow R-50s

EUDAMED

Class A (EU MDR)

Ref 5600Model CYBOW R-50SRef 5660

by DFI Co., Ltd.

Identity

Trade Name
CYBOW R-50S EUDAMED
DUS R-50S EUDAMED
Device Name
CYBOW R-50S EUDAMED
Model / Reference
CYBOW R-50S EUDAMED
5600 EUDAMED
5660 EUDAMED

Identifiers

Primary DI / UDI-DI
08806141302797 EUDAMED
08806141301912 EUDAMED
Basic UDI-DI
88061413UR6300H7 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

Cybow R-50s 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 (2)

  • EUDAMED 9fa96df2-74f0-4eb3-8ab1-eeef7ad79e80 61 fields · synced Jul 13, 2026
  • EUDAMED 499f7e15-70ec-4216-83db-d15b760235a0 61 fields · synced May 18, 2026