BEUDAMED
    10 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    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

    PERSONA TIBIAL ARTICULAR SURFACE PROVISIONAL

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JWH·December 10, 2017

    BD INSYTE¿ IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·August 2, 2019

    EASYTRAK 2

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·July 20, 2011

    CROSS-LINK-CLAMP F/R Ø6 PREASSMBL TAN DB

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code NKB·June 14, 2013

    ENDURANCE SZ 2 HIGH OFFSET

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·September 18, 2008