BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

    SILICONE ULTRAVIOLET ABSORBING POSTERIOR CHAMBER SINGLE PIEC

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 15, 2006

    SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 8, 2006

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    FDA Adverse Event
    Malfunction ·STAAR SURGICAL·Product code HQL·June 15, 2006

    SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code HQL·June 26, 2006

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·October 22, 2010

    FORTIFY VR, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code LWS·January 13, 2014

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 19, 2012

    SEE H-10

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL COMPANY·Product code HQL·October 10, 2012

    SEE H-10

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL COMPANY·Product code HQL·March 27, 2012

    BIOLOX® DELTA, CERAMIC FEMORAL HEAD, S, 36/-3.5, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·February 21, 2017