BEUDAMED
    3,463 results · 27ms · 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 Regulation: Us FDA ×

    LS2-SP

    FDA Adverse Event
    Malfunction ·MEDICAL DEVICE RESOURCE CORP.·Product code MUU·January 29, 2014

    VASERLIPO SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code QPB·January 9, 2023

    MICROAIRE

    FDA Adverse Event
    Death ·MICROAIRE SURGICAL INSTRUMENTS, LLC·Product code MUU·June 26, 2015

    VASERLIPO SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code QPB·January 5, 2023

    VASERLIPO SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code QPB·January 10, 2023

    VASERLIPO SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code QPB·October 21, 2022

    CANDYCANE 5MM 26CM LG

    FDA Adverse Event
    Malfunction ·MENTOR WW LLC·Product code MUU·October 25, 2016

    CANDYCANE 5MM 26CM LG

    FDA Adverse Event
    Malfunction ·MENTOR WW LLC·Product code MUU·October 25, 2016

    ACC III 3MM 32CM L HD CANNULA

    FDA Adverse Event
    Malfunction ·MENTOR WORLDWIDE LLC·Product code MUU·August 12, 2015

    MICROAIRE

    FDA Adverse Event
    Malfunction ·MICROAIRE SURGICAL INSTRUMENTS·Product code MUU·July 7, 2015

    PUREGRAFT 250

    FDA Adverse Event
    Malfunction ·CYTORI THERAPEUTICS, INC.·Product code MUU·August 19, 2015

    BECKER TEARDROP 3MM 26CM LG

    FDA Adverse Event
    MENTOR WORLDWIDE LLC·Product code MUU·June 11, 2014

    VASER LIPO SYSTEM

    FDA Adverse Event
    Injury ·SOUND SURGICAL TECHNOLOGIES·Product code MUU·February 12, 2010

    BECKER TEARDROP 5 MM, LARGE HANDLE CANNULA

    FDA Adverse Event
    Other ·BYRON MEDICAL·Product code MUU·June 3, 2010

    REVOLVE

    FDA Adverse Event
    Injury ·LIFECELL CORPORATION·Product code MUU·August 18, 2015

    ACC III 5MM 32CM L HD CANNULA

    FDA Adverse Event
    Malfunction ·MENTOR WORLDWIDE LLC·Product code MUU·August 12, 2015

    LIPOTOWER WITH ASPIRATION AND INFILTRATION

    FDA Adverse Event
    Malfunction ·MICROAIRE SURGICAL INSTRUMENTS·Product code MUU·August 28, 2015

    ELECTRIC CONSOLE FOR THE PAL SYSTEM

    FDA Adverse Event
    Malfunction ·MICROAIRE SURGICAL INSTRUMENTS·Product code MUU·September 3, 2015

    REVOLVE (OEM VERSION OF GID 700)

    FDA Adverse Event
    Injury ·THE GID GROUP INC.·Product code MUU·April 18, 2014

    BULLET TIP HOLW 5MM30CM PROBE

    FDA Adverse Event
    Injury ·MENTOR WORLDWIDE LLC·Product code MUU·June 4, 2014