BEUDAMED
    11 results · 38ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    JUGGERKNOT 1.4MM 1 #1 MB 10PK

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBI·January 20, 2020

    JUGGERKNOT 1.4MM 1 #1 MB 10PK

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBI·January 20, 2020

    JUGGERKNOT 1.4MM 1 #1 MB 10PK

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBI·January 20, 2020

    JUGGERKNOT 1.4MM 1 #1 MB 10PK

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code MBI·August 30, 2017

    JUGGERKNOT 1.4MM 1 #1 MB 10PK

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code MBI·August 30, 2017

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·January 11, 2013

    BIOGLUE SURGICAL ADHESIVE

    FDA Adverse Event
    Injury ·CRYOLIFE, INC.·Product code MUQ·December 1, 2010

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 3, 2014

    JUGGERKNOT 1.4MM 1 #1 MB 10PK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBI·December 12, 2014

    UNK BACTISEAL VENTRICULAR CATHETER

    FDA Adverse Event
    Injury ·Product code JXG·December 13, 2017

    JUGGERKNOT 1.4MM 1 #1 MB 10PK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBI·February 6, 2018