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

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    Filters FDA Adverse Event ×

    E.COM, SYMBIA E

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS USA, INC. MI GROUP·Product code IYX·March 15, 2012

    E.CAM

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SOLUTIONS USA, INC. MI GROUP·Product code KPS·January 7, 2014

    SYMBIA T-SERIES

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SOLUTIONS USA, INC. MI GROUP·Product code KPS·September 20, 2013

    E. CAM COMPUTER [510(K) K992731]

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC.·Product code IYX·April 20, 2001

    EVIS EXERAII BRONCHOVIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code EOQ·August 29, 2019

    ENDOVIVE TWO-PORT TTP JEJUNAL FEEDING TUBE CAP

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code KNT·June 30, 2014

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 9, 2013

    E-POLY 38MM RINGLOC MAX-ROM ACETABULAR LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·November 18, 2010