BEUDAMED
    9 results · 36ms · Sources: EU EUDAMED, US FDA

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    KOI(TM) INSTRUMENT TRAYS

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

    11MM TI CANNULATED TIBIAL NAIL-EX/330MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES SELZACH·Product code JDS·October 27, 2014

    PROLITE III TOWER AND PR AND HR HANDPIECE

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

    RF-Relief

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

    HANDLE FOR TORQUE LIMITING ATTACHMENT

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·August 12, 2021

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·October 13, 2022

    PRIMARY PLUMSET 2 CLAVES 272CM NDEHP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·April 7, 2014

    THERAPY ABLATION CATHETER

    FDA Adverse Event
    Malfunction ·IRVINE BIOMEDICAL, A ST. JUDE MED COMPANY·Product code OAD·October 1, 2010

    EXPRESS VASCULAR LD

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·December 20, 2012