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Lumix Surgery

by Fisioline SRL 8 variants

Ref LSURG1402, LSURG3001, LSURG3002Model LUMIX SURGERY

Lumix Surgery (LSURG1402) is a medical device (EU MDD Class IIb; EMDN category diode surgical laser) made by Fisioline SRL, registered in EUDAMED on 28 Apr 2026 (Basic UDI-DI B-08057949171089), active as of 22 Oct 2026.

Active European Union

CE MDD

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/MDD NumberB-08057949171089 Basic UDI-DI Date28 Apr 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
LUMIX SURGERY, LSURG1402, LSURG3001, LSURG3002
Primary DI / UDI-DI
08057949171089, 08057949171119, 08057949171126
Basic UDI-DI
B-08057949171089, B-08057949171119, B-08057949171126
EMDN code
Z12011016 Diode surgical laser
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000027924

Similar devices in this category

Other devices filed under DIODE SURGICAL LASER.

Other devices from Fisioline SRL

See all devices from Fisioline SRL →

Properties

Other properties (12, all answered No)