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GSL Workstation for BF

EUDAMED

Class A (EU MDR)

Ref 23GSLCPUBFXDXModel 23GSL10XBFF230DX

by Leica Biosystems Imaging, Inc.

Identity

Trade Name
GSL Workstation for BF EUDAMED
Device Name
CytoVision DX EUDAMED
Model / Reference
23GSL10XBFF230DX EUDAMED
23GSLCPUBFXDX EUDAMED

Identifiers

Primary DI / UDI-DI
00815477021003 EUDAMED
Basic UDI-DI
08498320358U EUDAMED
Direct Marketing DI
00815477021003 EUDAMED
EMDN Code
W0202050304 DIGITAL LABORATORY MICROSCOPES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Austria 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

Yes

EUDAMED

GSL Workstation for BF by Leica Biosystems Imaging, Inc. — 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

EUDAMED SRN
US-MF-000020547
Authorised Representative
CEpartner4U NL-AR-000000111

Sources (1)

  • EUDAMED 234ccf01-52c4-4a50-8ca5-75f303c164e6 61 fields · synced Jun 18, 2026