BEUDAMED
    58 results · 69ms · Sources: EU EUDAMED, US FDA

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    T.E.D. SEQUENTIAL COMPRESSION SLEEVES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REPROCESSED VENODYNE SEQUENTIAL COMPRESSION SLEEVES / WRAP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Plexus SCD110 Sequential Compression Device Sleeve

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REPROCESSED USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REPROCESSES USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KENDALL SCD RESPONSE-COMPRESS SYSTEM

    FDA Adverse Event
    Other ·WATERTOWN·Product code JOW·June 23, 2005

    SEQUENTIAL COMPRESSION SLEEVE

    FDA Adverse Event
    Injury ·KENDALL CO.·Product code JOW·July 2, 1996

    SCD COMPRESSION SYSTEM

    FDA Adverse Event
    Other ·WATERTOWN·Product code JOW·June 22, 2005

    KENDALL SCD 700 SERIES

    FDA Adverse Event
    Malfunction ·COVIDIEN LLC·Product code JOW·May 16, 2022

    KENDALL SCD COMPRESSION SYSTEM

    FDA Adverse Event
    Other ·WATERTOWN·Product code JOW·June 23, 2005

    KENDALL SCD

    FDA Adverse Event
    Malfunction ·TYCO HEALTHCARE/KENDALL·Product code JOW·August 5, 2003

    KENDALL

    FDA Adverse Event
    Injury ·KENDALL, A DIVISION OF TYCO HEALTHCARE GROUP·Product code JOW·May 23, 2005

    KENDALL SEQUENTIAL COMPRESSION DEVICE

    FDA Adverse Event
    Other ·TYCO HEALTHCARE / KENDALL·Product code JOW·August 18, 2005

    KENDALL SEQUENTIA COMPRESSION SYSTEM

    FDA Adverse Event
    Death ·TYCO HEALTHCARE/KENDALL·Product code JOW·July 11, 2005

    KENDAL SEQUENTIAL COMPRESSION DEVICE

    FDA Adverse Event
    Other ·TYCO HEALTHCARE / KENDALL·Product code JOW·August 18, 2005

    KENDAL SEQUENTIAL COMPRESSION DEVICE

    FDA Adverse Event
    Other ·TYCO HEALTHCARE / KENDALL·Product code JOW·August 18, 2005

    SCD EXPRESS SLEEVE K/L MEDIUM

    FDA Adverse Event
    Injury ·COVIDIEN·Product code JOW·July 9, 2009

    KENDALL SEQUENTIAL COMPRESSION DEVICE

    FDA Adverse Event
    Other ·TYCO HEALTHCARE/KENDALL·Product code JOW·August 18, 2005

    SCD RESPONSE-COMPRESSION SYSTEM

    FDA Adverse Event
    TYCO HEALTHCARE/KENDAL·Product code JOW·December 22, 2004