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

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    Filters FDA Adverse Event ×

    PUMP MMT-1780KPK 670G PATHWAY BLACK MG

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·January 29, 2019

    ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)

    FDA Adverse Event
    Malfunction ·ANGIOSCORE, INC·Product code LIT·November 18, 2015

    CONNECSCR F/UTN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·June 3, 2013

    KNEE IMPLANT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC. ORTHOPAEDIC DIVISION·Product code JWH·June 28, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008

    ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)

    FDA Adverse Event
    Injury ·ANGIOSCORE, INC·Product code LIT·March 29, 2016

    ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)

    FDA Adverse Event
    Malfunction ·ANGIOSCORE, INC·Product code LIT·November 26, 2015