BEUDAMED
    4 results · 22ms · 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 ×

    ISODUR PROSTHESIS HEAD 12/14 28MM M

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LPH·January 16, 2015

    PERMOBIL M300 CORPUS 3G

    FDA Adverse Event
    Malfunction ·PERMOBIL, INC.·Product code ITI·March 12, 2013

    NXSTAGE SYSTEM ONE

    FDA Adverse Event
    Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·May 9, 2008

    CONSULTA CRT-D

    FDA Adverse Event
    Death ·MEDTRONIC S.A.·Product code NIK·April 6, 2011