BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    NORELCO VIBRATING BOARD V900

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    SAFFRON NM GUIDING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Promisemed Safety Huber Needle

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ARGYLE SALEM SUMP TUBE WITH ANTI-REFLUX VALVE

    FDA Adverse Event
    Malfunction ·SHERWOOD DAVIS AND GECK·Product code KNT·August 29, 1996

    ABBOCATH-T 20G 1-1/4

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD·Product code FOZ·April 27, 2009

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·May 23, 2014

    ADVANCE(R) II TRADITIONAL TIBIAL INSERT

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JWH·November 13, 2012

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 10, 2010