BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·January 4, 2016

    LUX 1440

    FDA Adverse Event
    Malfunction ·PALOMAR MEDICAL TECHNOLOGIES, INC.·Product code GEX·May 5, 2012

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    CONSMA·Product code ITJ·April 29, 2013

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·May 10, 2011

    AMPLATZ GUIDEWIRE

    FDA Adverse Event
    BOSTON SCIENTIFIC·Product code KOG·July 24, 2008

    PROGREAT

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DQO·March 5, 2024

    TERUMO PROGREAT CATHETER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQO·February 6, 2023

    PROGREAT CATHETER

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DQO·January 6, 2024

    PROGREAT

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQO·April 15, 2025