BEUDAMED
    8 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.
    Filters Regulation: Us FDA ×

    HAEMOPHILUS TEST MEDIUM (HTM)AGAR

    FDA 510(k)
    FDA Class 2 ·Microbiology

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690197751·AK3 PS-C Insert Trial Size 2, 16mm

    GRASS MODEL NL FACIAL NERVE LOCATOR & MONITOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    EMIT QST PHENOBARBITAL ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    PLUM XLM W/DATAPORT

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·February 14, 2014

    VERIFLEX (LIBERTE) CORONARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·November 9, 2010

    HEARTMATE II LEFT VENTRICULAR ASSIST DEVICE

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·December 27, 2012

    BD BBL¿ HAEMOPHILUS TEST MEDIUM AGAR (HTM AGAR)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSO·November 15, 2021