BEUDAMED
    7 results · 29ms · 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 ×

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 19, 2024

    M2A-MAGNUM 42-50MM TAPER INSERT-6

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code KWA·November 16, 2016

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code CAW·May 3, 2013

    CORMET RESURFACING

    FDA Adverse Event
    Injury ·CORIN LTD.·Product code NXT·September 2, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 5, 2011

    M2A-MAGNUM MOD HD SZ 42MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 20, 2016

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORP.·Product code FDT·July 24, 2015