BEUDAMED
    10,000 results · 45ms · 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 Regulation: Us FDA ×

    MAGVENTURE MAGPROXP

    FDA Adverse Event
    Injury ·MAGVENTURE INC.·Product code GWF·January 4, 2019

    THYMATRON

    FDA Adverse Event
    Injury ·SOMATICS, LLC·Product code GXC·May 1, 2020

    VISIAN ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code MTA·September 23, 2014

    VISIAN ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code MTA·November 15, 2012

    ECT NARROW SELF-COMPRESSION PLATE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code HRS·May 5, 2000

    ECT INTERNAL FRACTURE HEXHEAD SCREWDRIVER

    FDA Adverse Event
    Malfunction ·ZIMMER INC·Product code HXX·August 4, 2011

    ECT INTERNAL FRACTURE FIXATION DRILL

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HTW·April 26, 2011

    ECT INTERNAL FRACTURE FIXATION DRILL

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HTW·November 18, 2011

    ECT INTERNAL FRACTURE FIXATION DRILL

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HTW·December 14, 2004

    ECT INTERNAL FRACTURE FIXATION DRILL

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HTW·August 30, 2012

    ECT INTERNAL FRACTURE DRILL BIT

    FDA Adverse Event
    Malfunction ·ZIMMER INC·Product code HTW·August 22, 2013

    ECT INTERNAL FRACTURE FIXATION DRILL

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HTW·March 6, 2009

    ECT INTERNAL FRACTURE DRILL BIT

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HTW·October 11, 2013

    ECT INTERNAL FRACTURE DRILL BIT

    FDA Adverse Event
    Malfunction ·ZIMMER INC·Product code HTW·April 1, 2016

    S5 IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·VOLCANO CORP·Product code IYO·October 13, 2008

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·August 26, 2011

    LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·MEDTRONIC EMERGENCY RESPONSE SYSTEMS·Product code LDD·June 14, 2004

    MEDTRONIC NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·Product code EZW·July 29, 2009

    PROGRAMMING COMPUTER

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·November 14, 2013

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·June 9, 2017