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

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    LABELING FOR MYO/WIRE II STERNOTOMY SUTURES

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

    T-WAVE ALTERNANS (TWA) ALGORITHM OPTION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Q-FIX SUTURE ANCHOR,1.8MM AND 2.8MM / DRILL, DRILL GUIDE AND OBTURATOR,1.8MM AND 2.8MM /BONE PUNCH,2.8MM AND KNOT PUSHER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ADVANCE(R) II TIBIAL BASE

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HRY·December 18, 2010

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD, CANBERRA HOUSE·Product code MKJ·January 23, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 14, 2014