BEUDAMED
    12 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    ASTRAL DC ADAPTER

    FDA Adverse Event
    Malfunction ·RESMED LTD·Product code CBK·June 30, 2017

    ASTRAL DC ADAPTER

    FDA Adverse Event
    Malfunction ·RESMED LTD·Product code CBK·November 14, 2017

    AMS MONARC SLING SYSTEM

    FDA Adverse Event
    Malfunction ·ASTORA WOMEN'S HEALTH LLC·Product code OTN·March 1, 2016

    AMS SPARC SLING SYSTEM

    FDA Adverse Event
    Malfunction ·ASTORA WOMEN'S HEALTH LLC·Product code OTN·January 8, 2016

    AMS MONARC SLING SYSTEM

    FDA Adverse Event
    Malfunction ·ASTORA WOMEN'S HEALTH LLC·Product code OTN·January 4, 2016

    AMS RETROARC RETROPUBIC SLING SYSTEM

    FDA Adverse Event
    Malfunction ·ASTORA WOMEN'S HEALTH LLC·Product code OTN·March 3, 2016

    AMS SPARC SLING SYSTEM

    FDA Adverse Event
    Malfunction ·ASTORA WOMEN'S HEALTH LLC·Product code OTN·January 22, 2016

    AMS ELEVATE ANTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE

    FDA Adverse Event
    Malfunction ·ASTORA WOMEN'S HEALTH LLC·Product code OTP·July 6, 2016

    AMS SPARC SLING SYSTEM

    FDA Adverse Event
    Malfunction ·ASTORA WOMEN'S HEALTH LLC·Product code OTN·May 24, 2016

    MINIARC

    FDA Adverse Event
    Malfunction ·ASTORA WOMEN'S HEALTH, LLC·Product code PAH·July 14, 2016

    AMS MONARC SLING SYSTEM

    FDA Adverse Event
    Malfunction ·ASTORA WOMEN'S HEALTH LLC·Product code OTN·April 13, 2016

    AMS MINIARC PRECISE SINGLE-INCISION SLING SYSTEM

    FDA Adverse Event
    Malfunction ·ASTORA WOMEN'S HEALTH LLC·Product code FTL·October 28, 2015