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Fluosoft Lm

by Fluoptics SAS

Ref FSLM-CL

Fluosoft Lm (FSLM-CL) is a Class IIa device made by Fluoptics SAS, registered in EUDAMED on 16 Jun 2023 (Basic UDI-DI ++B475FSAG), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++B475FSAG Basic UDI-DI +B475FSLM-CL0UDI-DIDate16 Jun 2023RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Fluosoft Lx/Lm
Model / reference
FSLM-CL
Primary DI / UDI-DI
+B475FSLM-CL0
Basic UDI-DI
++B475FSAG
EMDN code
Z119082 Various bioimaging and radiotherapy instruments - software accessories
Device class
Class IIa
Special device type
Software
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000403

Similar devices in this category

Other devices filed under VARIOUS BIOIMAGING AND RADIOTHERAPY INSTRUMENTS - SOFTWARE ACCESSORIES.

Other devices from Fluoptics SAS

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Properties

Other properties (14, all answered No)