BEUDAMED
    16 results · 40ms · 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 ×

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code GEI·October 2, 2009

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code GEI·October 14, 2009

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code GEI·October 14, 2009

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code GEI·October 14, 2009

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code GEI·October 16, 2009

    CLEARGLIDE EVH LONGVIEW W/SCIS

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code GEI·November 23, 2009

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code GEI·October 16, 2009

    CLEARGLIDE EVH SMALL W/SCISSOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code GEI·October 16, 2009

    CLEARGLIDE EVH LONGVIEW W/SCIS

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code GEI·November 9, 2009

    2520274-2013-01432

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code MNI·March 13, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·February 28, 2011

    IMPLANTIUM

    FDA Adverse Event
    Other ·DENTIUM CO., LTD.·Product code DZE·February 22, 2008

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code GEI·November 24, 2009

    CLEARGLIDE EVH SMALL W/SCISSOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code GEI·November 3, 2009

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code GEI·October 16, 2009

    BACFIX ROD, UNKNOWN

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code HSB·January 16, 2020