BEUDAMED
    6 results · 35ms · 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 Regulation: Us FDA ×

    ZETA SURGICAL INC.

    FDA registration
    ZETA SURGICAL INC.·3 products·🇺🇸 United States

    Powerheart AED G3 Automated External Defibrillator Model 9300A (Automatic). Cardiac Science AEDs are manufactured by: Manufacturing: Cardiac Science, Inc., 5474 Feltl Road, Minnetonka, MN 55343-7982.

    FDA Recall
    Terminated ·Cardiac Science Corporation·Product code MKJ·January 27, 2006

    PUMP MMT-1780KR 670G MG MEDI RECERT

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 20, 2022

    Powerheart AED G3 Automated External Defibrillator Model 9300E. Cardiac Science AEDs are manufactured by: Manufacturing: Cardiac Science, Inc., 5474 Feltl Road, Minnetonka, MN 55343-7982.

    FDA Recall
    Terminated ·Cardiac Science, Inc.·Product code MKJ·November 12, 2004

    Powerheart AED G3 Automated External Defibrillator Model 9300P Professional series). Cardiac Science AEDs are manufactured by: Manufacturing: Cardiac Science, Inc., 5474 Feltl Road, Minnetonka, MN 55343-7982.

    FDA Recall
    Terminated ·Cardiac Science, Inc.·Product code MKJ·November 12, 2004

    Powerheart AED G3 Automated External Defibrillator Model 9300A (Automatic). Cardiac Science AEDs are manufactured by: Manufacturing: Cardiac Science, Inc., 5474 Feltl Road, Minnetonka, MN 55343-7982.

    FDA Recall
    Terminated ·Cardiac Science, Inc.·Product code NPN·November 12, 2004