BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 9, 2012

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·January 15, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·December 8, 2010

    ENERGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 9, 2014

    VANGUARD CR FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·August 10, 2017

    REGENEREX PRIMARY TIBIAL TRAY

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBH·August 10, 2017

    BIOMET MODULAR FINNED STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·August 10, 2017

    REGENEREX PRIMARY PATELLA

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBH·August 10, 2017

    VANGUARD TIBIAL BEARING

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBH·August 10, 2017