BEUDAMED
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    Filters FDA Adverse Event ×

    ARTICUL/EZE BALL 28 +5 BR

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code JDI·June 6, 2014

    UNIDENTIFIED DEPUY IMPLANT OR INSTRUMENT

    FDA Adverse Event
    Injury ·Product code JWH·December 3, 2012

    ISERT ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS INC.·Product code HQL·September 2, 2010