BEUDAMED
    9 results · 15ms · 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 ×

    ZILVER 518 BILIARY SELF-EXPANDING STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 21, 2017

    KII 5X100 Z-THR CANNULA / SEAL 12/BOX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL·Product code GCJ·September 15, 2014

    MAESTRO DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HBB·April 19, 2011

    PREMICATH

    FDA Adverse Event
    Malfunction ·VYGON USA·Product code LJS·October 9, 2020

    PREMICATH

    FDA Adverse Event
    Malfunction ·VYGON USA·Product code LJS·October 9, 2020

    PREMICATH

    FDA Adverse Event
    Malfunction ·VYGON USA·Product code LJS·October 9, 2020

    PREMICATH

    FDA Adverse Event
    Malfunction ·VYGON USA·Product code LJS·October 9, 2020

    PREMICATH

    FDA Adverse Event
    Malfunction ·VYGON USA·Product code LJS·October 9, 2020

    ZILVER 518 SELF-EXPANDING STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 26, 2012