BEUDAMED
    12 results · 21ms · 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.

    DENTAURUM METAL BRACKETS

    FDA 510(k)
    FDA Class 1 ·Dental

    LP Low Profile

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746088438·DB BKT LP UL CEN 022 T+22 A+5 R=0

    SENTRY SCALE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PACE SAVER LITTLE JR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 7, 2010

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·July 14, 2010

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Injury ·INSULET CORP·Product code LZG·January 23, 2013

    CAN AM GOODNEIGH INS SYR 31G X1CC

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMF·December 6, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 3, 2014

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 27, 2010