BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    VENFLON 2 PNK 20GA IV CANNULA

    FDA Adverse Event
    Malfunction ·Product code FOZ·September 13, 2021

    PROMUS ELEMENT? PLUS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·May 29, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 16, 2011

    DEXTRUS 4137

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code DTB·August 21, 2008

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·May 9, 2019

    PEDICLE SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·May 9, 2019

    PEDICLE SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·May 9, 2019

    BAKRI TAMPONADE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNA·January 10, 2018