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GSL120 scan system BF FL

EUDAMED

Class A (EU MDR)

Ref 23GSL120BFF230DXModel 23GSL10XBFF230DXRef 23GSL120BFX230DX

by Leica Biosystems Imaging, Inc.

Identity

Trade Name
GSL120 scan system BF FL EUDAMED
GSL120 scan system BF EUDAMED
Device Name
CytoVision DX EUDAMED
Model / Reference
23GSL10XBFF230DX EUDAMED
23GSL120BFF230DX EUDAMED
23GSL120BFX230DX EUDAMED

Identifiers

Primary DI / UDI-DI
00815477020907 EUDAMED
00815477020914 EUDAMED
Basic UDI-DI
08498320358U EUDAMED
Direct Marketing DI
00815477020907 EUDAMED
00815477020914 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

No

EUDAMED

GSL120 scan system BF FL 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 (2)

  • EUDAMED e4c27abe-4f78-4c5e-b078-f4ba53b1846d 61 fields · synced Jul 17, 2026
  • EUDAMED dba3e3fc-9e77-49cf-b0a7-3173e0616dd2 61 fields · synced May 18, 2026