BEUDAMED
    9 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PENTA

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 10, 2012

    M2A 38MM MOD HD STD NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 20, 2013

    LIMITED USE LAPCLINCH GRASPER TIP

    FDA Adverse Event
    Other ·MICROLINE SURGICAL, INC.·Product code GEI·March 15, 2013

    ASR ACETABULAR CUPS 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 24, 2011

    SELOX ST 60

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code DTB·March 10, 2008

    COREVALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·May 28, 2015

    M2A 38MM MOD HD STD NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 3, 2013

    M2A-38 CUP NON FLARED SZ 54MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 3, 2013

    M2A 38MMX58MM CUP

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·August 13, 2012