BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PULSE GEN MODEL 1000

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·September 7, 2022

    PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code BTI·February 20, 2013

    SYNVISC

    FDA Adverse Event
    Injury ·Product code MOZ·January 13, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 31, 2014

    PS TIBIAL INSERTS SZ 4, 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·June 12, 2024

    LUTONIX 035 DRUG COATED BALLOON PTA CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (GFO)·Product code ONU·January 19, 2018

    LUTONIX 035 DRUG COATED BALLOON PTA CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (GFO)·Product code ONU·February 9, 2018

    LUTONIX 035 DRUG COATED BALLOON PTA CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (GFO)·Product code ONU·February 6, 2018

    LUTONIX 035 DRUG COATED BALLOON PTA CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (GFO)·Product code ONU·March 26, 2018

    LUTONIX 035 DRUG COATED BALLOON PTA CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (GFO)·Product code ONU·February 14, 2018