BEUDAMED
    8 results · 20ms · 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 ×

    GEM FLOW COUPLER DEVICE AND SYSTEM

    FDA Adverse Event
    Malfunction ·SYNOVIS SURGICAL INNOVATIONS·Product code MVR·October 8, 2015

    GEM FLOW COUPLER DEVICE AND SYSTEM

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code MVR·October 8, 2015

    GEM FLOW COUPLER DEVICE AND SYSTEM

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code MVR·October 8, 2015

    GEM FLOW COUPLER DEVICE AND SYSTEM

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code MVR·October 8, 2015

    GEM FLOW COUPLER DEVICE AND SYSTEM

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code MVR·October 8, 2015

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·January 30, 2013

    BIOMET ORTHOPEDICS

    FDA Adverse Event
    Injury ·BIOMET·Product code JDI·January 11, 2011

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL -NEUROMODULATION·Product code GZB·July 22, 2014