BEUDAMED
    8 results · 18ms · 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: Malfunction ×

    20/30 PRIORITY PACK INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR·Product code MAV·July 20, 2021

    GREENFIELD¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code DTK·March 12, 2013

    SM204 M-SERIES W/BIG WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·February 3, 2011

    20/30 PRIORITY PACK INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR·Product code MAV·April 20, 2021

    20/30 PRIORITY PACK INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR·Product code MAV·July 20, 2021

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·February 27, 2024

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·February 27, 2024

    20/30 PRIORITY PACK INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR·Product code MAV·March 2, 2022