BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    ACRO-POLY, INC. HANDPIECE/ANGLEHEAD ACCESSORIES FOR SURGICAL INSTUMENTS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    SeaSpine Spacer System - Hollywood

    FDA UDI
    Seaspine Orthopedics Corporation·10889981090036·Funnel Plunger

    ACCUPLACE (TM)

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    OP-CON SURG. INSTRUMENT #7

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 7, 2010

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·July 14, 2010

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

    FRESENIUS 2008K

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 27, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 3, 2013

    ALARIS SE PUMP

    FDA Adverse Event
    Other ·CAREFUSION CORP.·Product code FRN·December 14, 2010

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 27, 2010