BEUDAMED
    5 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GLENOID DRILL GUIDE HANDLE, LONG

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·March 29, 2021

    SERVO-I BASE UNIT

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·November 14, 2023

    ENRHYTHM DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code DXY·December 13, 2010

    NATURAL-KNEE II STEMMED TIBIAL BASEPLATE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·January 9, 2013

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LZG·July 9, 2014