BEUDAMED
    5 results · 24ms · 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 ×

    PORTEX® ULTRAPERC® SINGLE DILATOR TUBE

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD; INC.·Product code JOH·October 17, 2019

    QUICKDRAW VENOUS CANNULA

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DWF·April 11, 2013

    EASYTRAK 2

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·April 13, 2011

    ACCU-CHEK COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 27, 2008

    PORTEX BLUE LINE ULTRA SUCTIONAID PERCUTANEOUS DILATION TRACHEOSTOMY KIT

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code JOH·October 14, 2019