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GSL120 scan system BF

by Leica Biosystems Imaging, Inc. United States EUDAMED

Ref 23GSL120BFX230DXModel 23GSL10XBFF230DX EMDN W0202050304

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number08498320358U Basic UDI-DIDate16 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
CytoVision DX
Model / Reference
23GSL10XBFF230DX, 23GSL120BFX230DX
Primary DI / UDI-DI
00815477020914
Basic UDI-DI
08498320358U
Direct Marketing DI
00815477020914
EMDN Code
W0202050304 Digital laboratory microscopes
Device Class
Class A
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
US-MF-000020547
Authorised representative
AR Experts B.V. NL-AR-000023989

Other devices from Leica Biosystems Imaging, Inc.

See all devices from Leica Biosystems Imaging, Inc. →

Properties & raw data

Show properties, registry sources and raw records
  • Professional Testing
  • Surgical Instrument
Other properties (9)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • New Device: No

Sources (1)

  • EUDAMED dba3e3fc-9e77-49cf-b0a7-3173e0616dd2 61 fields · synced 24 Oct 2026