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

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    GENERAL PROCEDURE KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ArgenIS Titanium Abutments

    FDA 510(k)
    FDA Class 2 ·Dental

    ULTRATINE TRANSBLEPH

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 24, 2014

    5FR DL POWERPICC BASIC WITH MI AND TLS

    FDA Adverse Event
    Injury ·C. R. BARD INC. (BASD)·Product code FOZ·February 8, 2013

    ACRYSOF

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·January 5, 2011

    Ingenia Ambition S (781359), Ingenia Ambition X (781356) with Magnet Energization Device (MED), Philips MR systems are indicated for use as a diagnostic device. The purpose of the MED is to supply power to charge the magnet. MED is abbreviation for Magnet Energize Device

    FDA Recall
    Terminated ·Philips Medical Systems Nederlands Veenpluis 4-6 Best Netherlands·Product code LNH·March 25, 2019