BEUDAMED
    5 results · 19ms · 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 ×

    MALIS NSMF INS TI IRR BAY 8.75", 1.5MM

    FDA Adverse Event
    Malfunction ·Product code GEI·January 16, 2018

    IRRIGATION BI FCP STYLETS

    FDA Adverse Event
    Malfunction ·Product code GEI·January 16, 2018

    FLOGARD

    FDA Adverse Event
    Malfunction ·SHARP CORPORATION OSAKA JAPAN·Product code FRN·May 9, 2014

    PUREPOINT

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQF·October 19, 2012

    WEBSTER CS CATHETER WITH EZ-STEER TECHNOLOGY AND AUTO ID

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code DRF·August 17, 2010