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

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    Filters FDA Adverse Event ×

    PERIARTICULAR LOCKING SCREW 3.5MM

    FDA Adverse Event
    Malfunction ·ZIMMER INC·Product code HWC·September 4, 2015

    KINETRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·April 11, 2014

    PERIARTICULAR LOCKING SCREW 3.5MM

    FDA Adverse Event
    Malfunction ·ZIMMER INC·Product code HWC·November 6, 2015

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·March 19, 2014

    TM ANKLE TIBIAL BASE SIZE 4

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSN·November 26, 2020

    TALAR COMPONENT ORANGE SIZE 4 RIGHT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSN·January 8, 2021

    PROLONG TIBIAL INSERT SZ 4 +2

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSN·January 8, 2021

    KINETRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code MHY·July 30, 2012

    ECHOTIP ULTRA HIGH DEFINITION ULTRASOUND ACCESS NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·January 9, 2019

    ECHOTIP ULTRA HIGH DEFINITION ULTRASOUND ACCESS NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·September 26, 2018

    ECHOTIP ULTRA HIGH DEFINITION ULTRASOUND ACCESS NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·December 10, 2019

    ECHOTIP ULTRA HIGH DEFINITION ULTRASOUND ACCESS NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·July 30, 2019

    SNORE GUARD PRO

    FDA Adverse Event
    Malfunction ·RANIR, LLC·Product code LRK·June 30, 2014

    UNKNOWN REJUVENATE/ABGII MODULAR STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·March 13, 2013

    HEARTSTRING III PROXIMAL SEAL SYSTEM, 3.8 MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·January 27, 2011

    ECHOTIP ULTRA HIGH DEFINITION ULTRASOUND ACCESS NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·December 12, 2018

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·December 21, 2021

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·October 9, 2017

    ECHOTIP ULTRA HIGH DEFINITION ULTRASOUND ACCESS NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·October 20, 2023

    ECHOTIP ULTRA HIGH DEFINITION ULTRASOUND ACCESS NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·October 3, 2019