BEUDAMED
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    DEFIBTECH LLC

    FDA registration
    DEFIBTECH LLC·2 products·🇺🇸 United States

    DEFIBTECH, LLC

    FDA registration
    DEFIBTECH, LLC·2 products·🇺🇸 United States

    Lifeline AED DDU-100 semiautomatic external defibrillator used with the DBP-2800 Battery Pack, Manufactured by Defibtech, LLC. Seymour, CT 06483. The DBP-2800 battery pack is an accessory to the AED and does not have its own intended use. The AED is intended for use on victims of sudden cardiac arrest when the patient is unconscious, unresponsive and not breathing.

    FDA Recall
    Terminated ·Defibtech LLC·Product code MKJ·May 21, 2010

    ReviveR AED semiautomatic external defibrillator used with the DBP-2800 Battery Pack. Manufactured by Defibtech, LLC. Seymour, CT 06483. The DBP-2800 battery pack is an accessory to the AED and does not have its own intended use. The AED is intended for use on victims of sudden cardiac arrest when the patient is unconscious, unresponsive and not breathing.

    FDA Recall
    Terminated ·Defibtech LLC·Product code MKJ·May 21, 2010

    Defibtech DDP-100 Adult Defibrillation Pads For use with AED Models: Lifeline and Lifeline Auto (DDU-1:XX Series)- Indicated for use on victims of sudden cardiac arrest (SCA)

    FDA Recall
    Open, Classified ·Defibtech, LLC·Product code MKJ·October 14, 2024

    Defibtech DDP-200P: Pediatric Defibrillation Pads 0 For use with AED Models: Lifeline and Lifeline Auto (DDU-l XX Series)-Indicated for use on victims of sudden cardiac arrest (SCA.)

    FDA Recall
    Open, Classified ·Defibtech, LLC·Product code MKJ·October 14, 2024

    Defibtech DDP-2001: Adult Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, lifeline ECG, lifeline View (DDU-2XXX Series). -Indicated for use on victims of sudden cardiac arrest (SCA.)

    FDA Recall
    Open, Classified ·Defibtech, LLC·Product code MKJ·October 14, 2024

    Defibtech DDP-2002: Pediatric Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, Lifeline ECG, Lifeline View (DDU-2XXX Series -Indicated for use on victims of sudden cardiac arrest (SCA.)

    FDA Recall
    Open, Classified ·Defibtech, LLC·Product code MKJ·October 14, 2024

    Defibtech Sentry Semi-Automatic External Defibrilator (AED) sold as 'ReviveR AED' brand -Model DDU-100B (version 2.002 and earlier)

    FDA Recall
    Terminated ·Defibtech, LLC·Product code MKJ·February 17, 2007

    Defibtech Sentry Semi-Automatic External Defibrilator (AED) sold as 'Lifeline AED' brand -Model DDU-100A (version 2.002 and earlier)

    FDA Recall
    Terminated ·Defibtech, LLC·Product code MKJ·February 17, 2007

    LIFELINE AED

    FDA Adverse Event
    Malfunction ·DEFIBTECH, LLC·Product code MKJ·February 16, 2009

    LIFELINE AED

    FDA Adverse Event
    Death ·DEFIBTECH, LLC·Product code MKJ·March 30, 2009

    LIFELINE AED

    FDA Adverse Event
    Death ·DEFIBTECH, LLC·Product code MKJ·April 16, 2014

    REVIVER VIEW AED

    FDA Adverse Event
    Injury ·DEFIBTECH, LLC·Product code MKJ·April 11, 2014

    REVIVER AED

    FDA Adverse Event
    Death ·DEFIBTECH, LLC·Product code MKJ·April 3, 2014

    LIFELINE AED

    FDA Adverse Event
    Malfunction ·DEFIBTECH, LLC·Product code MKJ·March 3, 2010

    REVIVER AED

    FDA Adverse Event
    Malfunction ·DEFIBTECH, LLC·Product code MKJ·March 17, 2010

    LIFELINE AED

    FDA Adverse Event
    Death ·DEFIBTECH, LLC·Product code MKJ·March 4, 2010

    LIFELINE AED

    FDA Adverse Event
    Death ·DEFIBTECH, LLC·Product code MKJ·January 15, 2010

    LIFELINE AED

    FDA Adverse Event
    DEFIBTECH, LLC·Product code MKJ·March 10, 2010