BEUDAMED
    5 results · 18ms · 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 ×

    MEXFLEX TOTAL HIP SYSTEM

    FDA Adverse Event
    Other ·ALPHATEC SPINE, INC.·Product code JDI·August 29, 2006

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·January 22, 2013

    ADAPTA DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NVZ·December 14, 2010

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 10, 2014

    2.5MM GUIDE ROD W/STOP TROCAR TIP/230MM

    FDA Adverse Event
    Injury ·SYNTHES BALSTHAL·Product code FZX·November 29, 2016