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

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    ACE 8.0MM CANNULATED CANCELLOUS BONE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867138506·KOLBEL RETRTR BLADE,36MMX 68MMBLNT

    KOLBEL RETRTR BLADE,36MMX 68MMBLNT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GFA·February 20, 2025

    IMX ESTRADIOL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MODEL 8100 URODYNAMICS MEASURING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    KOLBEL RETRTR BLADE,36MMX 36MMBLNT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GFA·February 20, 2025

    SYNFIX MINI-OPEN IMPLANT COUPLING

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code MAX·January 23, 2013

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·November 10, 2010

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 10, 2014

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·February 6, 2017