BEUDAMED
    7 results · 28ms · 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 FDA Adverse Event ×

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·July 11, 2008

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·January 18, 2008

    PLATE BD CHROMAGAR O-157 20 EA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JSI·August 10, 2021

    PLATE BD CHROMAGAR O-157 20 EA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JSI·August 10, 2021

    DEXTRUS 4135

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·April 22, 2013

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORP·Product code LZG·March 29, 2011

    DORADO PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code LIT·July 1, 2008