BEUDAMED
    17 results · 45ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    NEXGEN LPS CEMENTED FEMORAL

    FDA Adverse Event
    Injury ·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code NJL·April 19, 2017

    FEMORAL COMPONENT OPTION SIZE F RIGHT

    FDA Adverse Event
    Injury ·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code NJL·December 19, 2017

    NEXGEN LPS-FLEX FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code NJL·March 10, 2017

    NEXGEN LPS-FLEX FEMORAL SIZE G RIGHT

    FDA Adverse Event
    Injury ·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code JWH·June 2, 2017

    NEXGEN LPS-FLEX - FEMORAL COMPONENT PRECOAT SIZE E LEFT

    FDA Adverse Event
    Injury ·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code NJL·March 17, 2017

    NEXGEN LPS-FLEX FEMORAL COMPONENT SIZE G RIGHT

    FDA Adverse Event
    Injury ·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code NJL·April 5, 2017

    NEXGEN LPS OPTION FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code NJL·April 6, 2016

    NEXGEN LPS-FLEX PRECOAT FEMORAL COMPONENT LEFT SIZE G

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code NJL·June 9, 2017

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·October 1, 2021

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·March 19, 2013

    ON-X PROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·ON-X LIFE TEHCNOLOGIES, INC.·Product code DYE·January 14, 2016

    ON-X MITRAL PROSTHETIC HEART VALVE

    FDA Adverse Event
    Other ·ON-X LIFE TECHNOLOGIES, INC.·Product code LWQ·July 14, 2011

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 19, 2013

    MAYFIELD MODIFIED SKULL CLAMP

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION·Product code HBL·June 11, 2008

    CONFIENT

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·April 15, 2011

    ONX AORTIC ANATOMIC EXT 27/29

    FDA Adverse Event
    Injury ·ONX LIFE TECHNOLOGIES, INC.·Product code LWQ·March 14, 2017

    ONX AORTIC ANATOMIC EXT 23

    FDA Adverse Event
    Injury ·ON-X LIFE TECHNOLOGIES, INC.·Product code LWQ·August 26, 2020