BEUDAMED
    7 results · 26ms · 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.

    OMNISONICS ULTRASONIC PROBES

    FDA 510(k)
    FDA Unclassified ·Unknown

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993628·anteriors; shade BL4; mould CM

    AGE Automatic Wrist Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OLYMPUS ISE MODULE FOR AU5000

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·March 7, 2013

    XIA II PA ADUSTMENT DRIVER

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code LXH·January 6, 2011

    XENFORM

    FDA Adverse Event
    Other ·TEI BIOSCIENCES, INC.·Product code FTM·July 28, 2014