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

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    AMSCO 600 Steam Sterilizer

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RIGIDLOOP

    FDA UDI
    S.B.M·03760304680212·The RIGIDLOOP device consists of an adjustable ...

    RIGIDLOOP

    FDA Adverse Event
    Malfunction ·S.B.M. SAS·Product code MBI·September 14, 2023

    K231485

    FDA Adverse Event
    Malfunction ·BETA BIONICS, INC.·Product code QFG·October 25, 2025

    ImPACT Version 4

    FDA 510(k)
    FDA Class 2 ·Neurology

    MEDTRONIC MINIMED COUNTACH INFUSION SET, MODEL 313

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RIGIDLOOP

    FDA Adverse Event
    Injury ·S.B.M. SAS·Product code MBI·May 6, 2022

    GE OEC 9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·November 13, 2008

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·September 2, 2011

    TENDRIL STS

    FDA Adverse Event
    Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·July 18, 2013

    RIGIDLOOP

    FDA Adverse Event
    Malfunction ·S.B.M. SAS·Product code MBI·October 31, 2023