BEUDAMED
    5 results · 28ms · 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 ×

    SPEEDPASS DISPOSABLE SUTURE LARIAT W/ NITINOL WIRE 45 DEGREE UP

    FDA Adverse Event
    Malfunction ·BIOMET SPORTS MEDICINE·Product code MDM·June 23, 2010

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·August 15, 2019

    TIMESH X-DRIVE SELF TAPPING 1.5 MM SCREW

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JEY·June 10, 2014

    HOMECHOICE CYCLER-REFURBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·October 11, 2010

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FSA·December 10, 2012