BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    MELANITE I

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228725061·GC Initial™ IQ/Effect Ingot C2-M, 5 pcs. X 2g

    GC Initial™

    FDA UDI
    Gc America Inc.·15400556709761·GC Initial™ IQ/Effect Ingot C2-M, 5 pcs. X 2g

    BD Cathena Safety IV Catheter

    FDA 510(k)
    FDA Class 2 ·General Hospital

    EXACTRAC 5.5

    FDA 510(k)
    FDA Class 2 ·Radiology

    2.4MM LOCKING SCREW SLF-TPNG WITH STARDRIVE RECESS 18MM

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code HRS·August 7, 2014

    PLUM A+ DRIVER REFUR

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·April 18, 2014

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAAN DIEGO, INC.·Product code GJS·December 12, 2012

    PROTACK

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GDW·September 30, 2010

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·September 15, 2025