BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    ARTHOPOR I & II ACETABULAR CUP/ARTHOPOR II OBLONG ACETABULAR CUP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Zuma

    FDA UDI
    Seaspine Orthopedics Corporation·10889981097110·Zuma 6.0mm Bone Screw Caddy

    CODMAN NEUROLASE LASER SYSTEM/MODIFICATION

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

    MIRAGE COMPLETE KIT AND MIRAGE ABC KIT

    FDA 510(k)
    FDA Class 2 ·Dental

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·February 11, 2013

    TENDRIL ST

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 24, 2014