BEUDAMED
    9 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Atlas Spine Expandable Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SMOOTH STEINMANN PINS, TROCAR POINT

    FDA UDI
    Biomet Orthopedics, LLC·00887868016769·

    DURABLUE STERILIZATION (AMSCO V-PRO) WRAP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    KARL STORZ FLEXIBLE VIDEO-URETHRO-CYSTOSCOPE SYSTEM

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

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 25, 2025

    VERSAFITCUP CC TRIO ACETABULAR SHELL Ø 48

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·December 30, 2016

    PROMETRA PROGRAMMABLE PUMP

    FDA Adverse Event
    Injury ·FLOWONIX MEDICAL, INC·Product code LKK·October 8, 2014

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 13, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 15, 2011