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

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    FC-100 FEMORAL CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MICHELANGELO BUNION SYSTEM - MABS, MODEL: MA6000

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MyDay (Stenfilcon A) ASPHERE, MyDay (Stenfilcon A) TORIC, MyDay (Stenfilcon A) MULTIFOCAL, MyDay (Stenfilcon A) MULTIFOCAL TORIC

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·June 10, 2014

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code HET·October 20, 2010

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·December 31, 2012