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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    MAMEX DC MAG MG12

    FDA 510(k)
    FDA Class 2 ·Radiology

    MIC-BIO-PLATE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    HYPERBARIC AMERICA, LLC, PRESIDENTIAL MONOPLACE HYPERBARIC CHAMBER SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ACCURUS 800CS

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·April 9, 2014

    POSEY PERSONAL ALARM LOUD

    FDA Adverse Event
    Malfunction ·DONGGUAN POSEY MEDICAL DEVICE LTD.·Product code KMI·October 19, 2010

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·December 18, 2012