BEUDAMED
    11 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    TSRH SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·SOFAMOR DANEK MANUFACTURING·Product code JDN·June 4, 1999

    ITREL

    FDA Adverse Event
    Other ·MEDTRONIC INC.·Product code GZB·March 28, 2001

    PERRY

    FDA Adverse Event
    Other ·ANSELL PERRY·Product code KGO·March 20, 1998

    UNK

    FDA Adverse Event
    Other ·JOHNSON & JOHNSON MEDICAL, INC.·Product code KGO·April 3, 1998

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·October 2, 2024

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·January 14, 2026

    URETEX SUPPORT PP KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code FTL·April 3, 2013

    UNKNOWN ZIMMER SHOULDER

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code HSD·March 31, 2011

    CONTAK RENEWAL 3 RF

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code NIK·May 8, 2008

    C8701, S ALEXIS LAP SYS W/ KII FIOS 5/BX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code GCJ·November 14, 2016

    INFUSAID IMPLANTABLE INFUSION PUMP

    FDA Adverse Event
    Injury ·STRATO/INFUSAID, INC.·Product code LKK·July 17, 1997