BEUDAMED
    77 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

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

    FORTIFY ASSURA DR ICD, US

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·June 13, 2016

    FORTIFY ASSURA VR ICD_IDE_US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·March 29, 2017

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

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

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

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

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

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

    ELLIPSE VR ICD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·March 29, 2017

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

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

    COLLAMER ULTRAVIOLET ABSORBING POSTERIOR CHAMBER THREE PIECE

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

    CD2257-40Q FORTIFY ASSURA DR ICD_IDE_US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NVZ·June 14, 2017

    FORTIFY ASSURA VR ICD_IDE_US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code NVZ·October 31, 2017

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

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

    UNIFY ASSURA CRT-D RF HV

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWS·March 29, 2019

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

    FDA Adverse Event
    Injury ·STAAR SURGICAL CO.·Product code HQL·June 21, 2006

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIEC

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

    DELTA CER HEAD 12/14 36MM +1.5

    FDA Adverse Event
    Injury ·8010379 DEPUY INTL., LTD.·Product code LZO·March 5, 2013

    INJECTION NEEDLE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code KOG·February 15, 2011

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MPRI·Product code LWP·August 7, 2014

    FORTIFY ST DR, U1.6 SJ4 ID

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code LWS·January 18, 2017

    FORTIFYASSURA DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·January 3, 2017