BEUDAMED
    42 results · 52ms · 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.

    LAERDAL SILICONE RESUSCITATOR

    FDA Adverse Event
    Malfunction ·LAERDAL MEDICAL A/S·Product code BTM·May 8, 2008

    STIFNECK SELECT COLLAR

    FDA Adverse Event
    LAERDAL MEDICAL CORP·Product code IQK·September 26, 2003

    LAERDAL SILICONE RESUSCITATOR

    FDA Adverse Event
    Malfunction ·LAERDAL MEDICAL A/S·Product code BTM·July 17, 2013

    LAERDAL SILICONE RESUSCITATOR

    FDA Adverse Event
    Malfunction ·LAERDAL MEDICAL, A.S.·Product code BTM·September 1, 2010

    THE BAG II DISPOSABLE RESUSCITATOR

    FDA Adverse Event
    LAERDAL MEDICAL A.S.·Product code BTM·May 29, 2014

    V-VAC MANUAL ASPIRATOR

    FDA Adverse Event
    Death ·LAERDAL MEDICAL A.S.·Product code JCX·January 23, 2008

    Laerdal "HeartStart Defibrillator", model M5067A, under Laerdal brand for Laerdal Medical Corp, Wappingers Falls, NY and is sold outside the U.S. The HeartStart is an automated external defibrillator for use on site and consists of a computer with digital interface and cartridge containing pads.

    FDA Recall
    Terminated ·Philips Medical Systems·Product code MKJ·April 30, 2008

    AUTOMATIC EXTERNAL DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·LAERDAL MEDICAL CORP.·Product code MKJ·July 22, 1996

    HEARTSTART SEMIAUTOMATIC DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·LAERDAL MEDICAL CORP.·Product code MKJ·July 18, 1996

    LAERDAL INFLATE-A-SHIELD

    FDA Adverse Event
    Malfunction ·LAERDAL MEDICAL CORP.·Product code CBP·January 30, 2002

    LAERDAL INFLATE-A-SHIELD

    FDA Adverse Event
    Malfunction ·LAERDAL MEDICAL CORP.·Product code CBP·January 30, 2002

    LAERDAL INFLATE-A-SHEILD

    FDA Adverse Event
    Malfunction ·LAERDAL MEDICAL CORP.·Product code CBP·January 30, 2002

    LAERDAL HEARTSTART 3000

    FDA Adverse Event
    Injury ·LAERDAL MEDICAL CORP·Product code MKJ·July 21, 2000

    ADULT SILICONE RESUSCITATOR

    FDA Adverse Event
    Death ·LAERDAL MEDICAL CORP.·Product code BTM·March 3, 1994

    HEARTSTART SEMI-AUTOMATED DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·LAERDAL MEDICAL CORP.·Product code LDD·February 11, 1994

    V-VAC MANUAL ASPIRATOR

    FDA Adverse Event
    Injury ·LAERDAL MEDICAL CORP.·Product code BTA·June 8, 2000

    HEARTSTART 2000

    FDA Adverse Event
    Malfunction ·LAERDAL MEDICAL CORP.·Product code MKJ·June 22, 2000

    LAERDAL SUCTION UNIT

    FDA Adverse Event
    Malfunction ·LAERDAL MEDICAL CORP.·Product code BTA·March 11, 2003

    HEARTSTART SEMIAUTOMATIC DEFIBRILLATOR

    FDA Adverse Event
    Death ·LAERDAL MEDICAL CORP.·Product code MKJ·March 8, 1995

    LAERDAL HEARTSTART 1000

    FDA Adverse Event
    Malfunction ·LAERDAL MEDICAL CORP.·Product code MKJ·October 16, 2000