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Fluopod

by Fluoptics SAS

Ref FMSA

Fluopod (FMSA) is a Class I device made by Fluoptics SAS, registered in EUDAMED on 16 Jun 2023 (Basic UDI-DI ++B475FMSACF), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++B475FMSACF Basic UDI-DI +B475FMSA0UDI-DIDate16 Jun 2023RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
FMSA
Primary DI / UDI-DI
+B475FMSA0
Basic UDI-DI
++B475FMSACF
Direct marketing DI
+B475FMSA0
EMDN code
Z119080 Various bioimaging and radiotherapy instruments - hardware accessories
Device class
Class I
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 - HARDWARE ACCESSORIES.

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Properties

Other properties (14, all answered No)