BEUDAMED
    10 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MYNXGRIP (6F/7F) VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code MGB·August 31, 2016

    MYNXGRIP (6F/7F) VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code MGB·August 31, 2016

    MYNXGRIP (6F/7F) VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code MGB·August 31, 2016

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·Product code OYC·March 13, 2013

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 18, 2011

    CONTROL CABLE W/CABLE SLEEVE

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDQ·February 20, 2008

    MYNXGRIP (6F/7F) VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code MGB·August 31, 2016

    DISP.TROCAR THRD.W.DILATING PIN 12/110MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GCJ·July 9, 2019

    MESH SOFRADIM - PARIETEX¿ OPTIMIZED COMPOSITE MESH

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·April 19, 2019

    18.0MM, MINI ACUTRAK 2® BONE SCREW

    FDA Adverse Event
    Malfunction ·ACUMED, LLC·Product code HWC·July 19, 2022