BEUDAMED
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    LifeSync Corporation

    FDA registration
    LifeSync Corporation·12 products·🇺🇸 United States

    LIFESYNC LEADWEAR

    FDA Adverse Event
    Other ·LIFESYNC CORPORATION·Product code DSA·July 1, 2009

    LIFESYNC ECG SYSTEM

    FDA Adverse Event
    Death ·LIFESYNC CORPORATION·Product code DRT·February 21, 2008

    LIFESYNC ECG SYSTEM

    FDA Adverse Event
    Malfunction ·LIFESYNC CORPORATION·Product code DRT·December 14, 2007

    LIFESYNC ECG SYSTEM

    FDA Adverse Event
    Malfunction ·LIFESYNC CORPORATION·Product code DRT·December 14, 2007

    LIFESYNC ECG SYSTEM

    FDA Adverse Event
    Malfunction ·LIFESYNC CORPORATION·Product code DRT·December 14, 2007

    LIFESYNC LEADWEAR

    FDA Adverse Event
    Other ·LIFESYNC CORPORATION·Product code DSA·January 9, 2009

    LIFESYNC ECG SYSTEM

    FDA Adverse Event
    Malfunction ·LIFESYNC CORPORATION·Product code DRT·December 14, 2007

    LIFESYNC ECG SYSTEM

    FDA Adverse Event
    Malfunction ·LIFESYNC CORPORATION·Product code DRT·December 14, 2007

    LIFESYNC ECG SYSTEM

    FDA Adverse Event
    Malfunction ·LIFESYNC CORPORATION·Product code DRT·December 14, 2007

    LIFESYNC ECG SYSTEM

    FDA Adverse Event
    Malfunction ·LIFESYNC CORPORATION·Product code DRT·December 18, 2007

    SMART BATTERY

    FDA Adverse Event
    Malfunction ·LIFESYNC CORPORATION·Product code DRG·August 5, 2010

    LS-202 Large LeadWear Combo Pack - Disposable ECG Monitoring component intended for use as a radiofrequency signal transmitter and receiver of electrocardiograph physiological signals which are displayed on the ECG monitors of various manufacturers' systems that have been validated for compatibility.

    FDA Recall
    Terminated ·Lifesync Corporation·Product code DRG·December 13, 2007

    LS-232 Large 12 LeadWear Single Pack - Disposable ECG Monitoring component intended for use as a radiofrequency signal transmitter and receiver of electrocardiograph physiological signals which are displayed on the ECG monitors of various manufacturers' systems that have been validated for compatibility.

    FDA Recall
    Terminated ·Lifesync Corporation·Product code DRG·December 13, 2007

    LifeSync ECG System - Disposable leadwear, Ls-222, Ls-223

    FDA Recall
    Terminated ·GMP Companies/Lifesync Corporation·Product code DRG·January 10, 2007

    LIFESYNCH WIRELESS PATIENT TRANSCEIVER

    FDA Adverse Event
    LIFESYNCH CORPORATION·Product code DRG·June 16, 2010

    LYNX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code OTN·July 14, 2021