BEUDAMED
    105 results · 24ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Death ×

    M SERIES

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORP.·Product code MKJ·November 24, 2004

    AED PLUS

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 4, 2007

    M SERIES

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORP.·Product code MKJ·November 24, 2004

    UNI-VENT, MODEL 731

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORPORATION·Product code CBK·April 21, 2021

    UNI-VENT, MODEL 731

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORPORATION·Product code CBK·April 21, 2021

    UNI-VENT, MODEL 731

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORPORATION·Product code CBK·April 21, 2021

    M SERIES

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 15, 2010

    M SERIES

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 15, 2010

    ASSY,MAIH, 3.0 DIA, W/SWITCH

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORPORATION·Product code LDD·November 2, 2015

    M SERIES

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORPORATION, WORLD WIDE HEADQUARTERS·Product code MKJ·September 17, 2010

    PD1200 DEFIBRILLATOR/PACEMAKER

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORP.·Product code LDD·March 31, 1999

    SOLID GEL MFE, ADULT

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORP.·Product code MLN·May 5, 1999

    SOLID GEL MFE, ADULT

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORP.·Product code MLN·May 5, 1999

    SOLID GEL MFE, ADULT

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORP.·Product code MLN·May 5, 1999

    1220908-2001-01522

    FDA Adverse Event
    Death ·October 31, 2001

    1220908-2017-00825

    FDA Adverse Event
    Death ·April 14, 2017

    1220908-2017-01009

    FDA Adverse Event
    Death ·April 28, 2017

    1220908-2017-01449

    FDA Adverse Event
    Death ·June 15, 2017

    UNI-VENT, MODEL 731

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORPORATION·Product code CBK·April 23, 2020

    X SERIES

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 29, 2016