BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    EAGLE

    FDA 510(k)
    FDA Class 2 ·Dental

    BASE

    FDA UDI
    Nuvasive, Inc.·00887517700476·BASE Guide, I

    PULMANEX DISPOSABLE PRESSURE MANOMETER, MODEL 50-5000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Extremity Medical Calcaneal Osteotomy Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD ANGIOCATH¿ IV CATHETER 22 G X 1"

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·September 13, 2017

    OCTRODE

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL NEUROMODULATION·Product code GZB·June 19, 2014

    CRYSTALENS ACCOMMODATING IOL

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code NAA·February 6, 2013

    PANTA IMPLANT SET

    FDA Adverse Event
    Malfunction ·NEWDEAL S.A.S.·Product code JDS·December 14, 2010

    BD ANGIOCATH¿ IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FOZ·August 8, 2017