BEUDAMED
    4 results · 32ms · 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 ×

    CUP: MPACT DOUBLE MOBILITY ACETABULAR SHELL 48

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·July 7, 2020

    LENSX LASER SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - LENSX LASERS, INC.·Product code OOE·March 21, 2014

    CAPSUREFIX NOVUS MRI

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code NVN·October 31, 2012

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code NJE·August 23, 2010