BEUDAMED
    12 results · 23ms · Sources: EU EUDAMED, US FDA

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    POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SeaSpine Spacer System - Hollywood

    FDA UDI
    Seaspine Orthopedics Corporation·10889981089740·Straight Pituitary, 5mm

    WILTEK ELECTROCAUTERY ACTIVE CORD

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Medline Reusable Sterilization Wrappers

    FDA 510(k)
    FDA Class 2 ·General Hospital

    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

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

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

    GRANUFLO

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

    STENOSCOP

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

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·December 3, 2010

    TRANSEND GUIDEWIRE

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