BEUDAMED
    9 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·June 6, 2014

    NELLCOR N20PA

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code DQA·November 29, 2012

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·September 30, 2010

    VANGUARD FEMORAL POSTERIOR AUGMENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 23, 2018

    VANGUARD FEMORAL POSTERIOR AUGMENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 23, 2018

    VANGUARD FEMORAL DISTAL AUGMENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 23, 2018

    VANGUARD SSK INTERLOK FEMORAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 12, 2017

    VANGUARD POSTERIOR STABILIZED TIBIAL BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 12, 2017

    BIOMET SPLINED KNEE STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 12, 2017