BEUDAMED
    7 results · 18ms · 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 ×

    TUBE CEV649-5B DIA 5MM 350MM [MXI/XOM]

    FDA Adverse Event
    Malfunction ·XOMED MICROFRANCE MFG·Product code GEI·February 26, 2014

    EDWARDS ESHEATH INTRODUCER SET

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·December 6, 2021

    EDWARDS TF SHEATH UNKNOWN

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·October 30, 2021

    SPRINT FIDELIS

    FDA Adverse Event
    Death ·MPRI·Product code LWS·March 7, 2013

    CLIP, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·February 16, 2011

    KAPPA 700 D

    FDA Adverse Event
    Malfunction ·IPG MFG SWITZERLAND·Product code NVZ·August 8, 2014

    MICROFRANCE® INSTRUMENT

    FDA Adverse Event
    Malfunction ·XOMED MICROFRANCE MFG·Product code GEI·April 15, 2015