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

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    3005075853-2019-17600

    FDA Adverse Event
    Malfunction ·March 27, 2019

    NRFIT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·September 4, 2020

    CADD CASSETTE RESERVOIR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·August 6, 2020

    CADD MEDICATION CASSETTE RESERVOIR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·September 9, 2020

    NRFIT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·June 16, 2020

    G/K FEM NAIL LEFT 10MMX38CM

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC.·Product code JDS·April 1, 1999

    LIFEPAK 5 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL CORP.·Product code MKJ·August 29, 1997

    BONE HOG

    FDA Adverse Event
    Injury ·BIOMEDICAL ENTERPRISES INC,·Product code HWK·February 26, 2001

    M2A-MAGNUM PF CUP 50ODX44ID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 17, 2021

    M2A-MAGNUM MOD HD SZ 44MM 44MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 17, 2021

    PERCEPT

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·May 9, 2022

    SLIDING MECHANISM

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTD·December 5, 2018