BEUDAMED
    153 results · 31ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Malfunction ×

    LUMENIS BE INC.

    FDA Adverse Event
    Malfunction ·LUMENIS BE INC·Product code HLJ·November 30, 2022

    THERMOCOOL® SMART TOUCH¿ ELECTROPHYSIOLOGY CATHETER

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC.·Product code LPB·September 6, 2019

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·May 18, 2026

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·April 24, 2025

    COHERENT VP SELECT

    FDA Adverse Event
    Malfunction ·LUMENIS, INC.·Product code GEX·February 3, 2012

    SLIMLINE

    FDA Adverse Event
    Malfunction ·LUMENIS, INC.·Product code LNX·February 18, 2010

    SHARPLAN

    FDA Adverse Event
    Malfunction ·LUMENIS, INC.·Product code GEX·March 18, 2010

    DUOTOME SIDELITE

    FDA Adverse Event
    Malfunction ·LUMENIS, INC.·Product code GEX·June 25, 2010

    SLIMLINE EZTM

    FDA Adverse Event
    Malfunction ·LUMENIS, INC.·Product code GEX·June 11, 2010

    SELECTA DUET

    FDA Adverse Event
    Malfunction ·LUMENIS, INC.·Product code HQF·September 9, 2015

    LUMENIS MOSES 200 B/F/L

    FDA Adverse Event
    Malfunction ·LUMENIS, INC.·Product code GEX·October 22, 2021

    ELITE E85

    FDA Adverse Event
    Malfunction ·LUMENIS, INC.·Product code HQB·December 18, 2003

    OPHTHALMIC ARGON LASER

    FDA Adverse Event
    Malfunction ·LUMENIS INC.·Product code HQF·May 18, 2007

    SELECTA DUET

    FDA Adverse Event
    Malfunction ·LUMENIS INC.·Product code GEX·June 22, 2021

    SLIM LINE EZ 550

    FDA Adverse Event
    Malfunction ·LUMENIS, INC.·Product code GEX·November 25, 2009

    LUMENIS MOSES 120W LASER

    FDA Adverse Event
    Malfunction ·LUMENIS, INC.·Product code GEX·December 20, 2018

    SLIMLINE

    FDA Adverse Event
    Malfunction ·LUMENIS, INC.·Product code GEX·November 4, 2009

    NOVUS 2000

    FDA Adverse Event
    Malfunction ·LUMENIS INC·Product code HQF·May 5, 2005

    SHARPLAN

    FDA Adverse Event
    Malfunction ·LUMENIS, INC.·Product code GEX·May 27, 2005

    LUMENIS PULSE 100H

    FDA Adverse Event
    Malfunction ·LUMENIS, INC.·Product code GEX·September 1, 2020