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UF- Fluorocell SF

EUDAMED

Class A (EU MDR)

Ref AV083519

by Sysmex Corporation

Identity

Trade Name
UF- Fluorocell SF EUDAMED
Device Name
UF- Fluorocell SF EUDAMED
Model / Reference
AV083519 EUDAMED

Identifiers

Primary DI / UDI-DI
14987562509062 EUDAMED
Basic UDI-DI
4987562UF-FluorocellSFMC EUDAMED
EMDN Code
W01010999 MULTIPLE PARAMETERS URINE TESTING - OTHER 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

Yes

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

UF- Fluorocell SF by Sysmex Corporation — 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
Sysmex Corporation
EUDAMED SRN
JP-MF-000014037
Authorised Representative
Sysmex Europe SE DE-AR-000022333

Sources (1)

  • EUDAMED 11d1a398-3796-49d7-99db-f8ee5ee8f9de 61 fields · synced Jun 18, 2026