BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    ALPHADENT LIGHT ACTIVATED ORTHODONTIC ADHESIVE BONDING SYSTEM WITH FLUORIDE

    FDA 510(k)
    FDA Class 2 ·Dental

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515243439·Ostrum Antrum Punch, str

    DELTA CER HEAD 12/14 36MM +12

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LZO·May 31, 2024

    INTRODUCER CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CVIS INSIGHT IMAGING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNICEL® DXC 600 PRO SYNCHRON® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code CGA·December 22, 2010

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code ILS·January 30, 2013

    MITEK DRILL PIN WITH EYELET .094X14

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code NBH·July 15, 2014