BEUDAMED
    7 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LATERAL STRAIGHT STEM 15.0 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWB·March 28, 2012

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 22, 2013

    PRISM REACTION TRAYS

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·December 14, 2010

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 9, 2014

    SULOX-HD 32 M 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·April 23, 2019

    SULOX, HEAD, M¸ 32/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWB·August 3, 2018

    SULOX-HEAD 28 M 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LPH·April 4, 2019