BEUDAMED
    6 results · 36ms · 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 ×

    AVENIR MÜLLER, STEM, STANDARD, UNCEMENTED, HA, 3, TAPER 12/14

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LZO·December 11, 2017

    AVENIR MÜLLER, STEM, LATERAL, UNCEMENTED, HA, 4, TAPER 12/14

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LZO·December 8, 2017

    AVENIR MÜLLER, STEM, LATERAL, UNCEMENTED, HA, 4, TAPER 12/14

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LZO·December 22, 2017

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 9, 2013

    PROMOS GLENOID

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code HSD·November 23, 2010

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 1, 2014