BEUDAMED
    10 results · 35ms · 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

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·May 6, 2014

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 22, 2010

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·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