BEUDAMED
    3 results · 20ms · 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 ×

    MA204

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·January 30, 2013

    RUSCH FOLEY CATHETER 100%SILICONE 2WAY 5CC 18F

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code EZL·November 24, 2010

    CAPSUREEPI

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code DTB·July 15, 2014