BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MEDEX¿ CLEAR-CUFF PRESSURE INFUSOR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code KZD·June 14, 2017

    TRULIANT TIB IMP PSC INSERT SZ 3, 15MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 17, 2024

    MEDEX¿ CLEAR-CUFF PRESSURE INFUSOR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code KZD·June 14, 2017

    UNKNOWN DEPUY BONE CEMENT

    FDA Adverse Event
    Injury ·9610921 DEPUY CMW·Product code LOD·April 2, 2013

    ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·March 22, 2011

    HI-TORQUE WHISPER MS GUIDE WIRE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code DQX·April 17, 2008

    MEDEX¿ CLEAR-CUFF PRESSURE INFUSOR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code KZD·June 14, 2017

    MEDEX¿ CLEAR-CUFF PRESSURE INFUSOR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code KZD·June 14, 2017

    NEOPUFF INFANT RESUSCITATOR

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTL·January 26, 2012

    MEDEX¿ CLEAR-CUFF PRESSURE INFUSOR

    FDA Adverse Event
    Death ·SMITHS MEDICAL ASD, INC.·Product code KZD·June 14, 2017