BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    VIPER PRIME™ additions to the VIPER® System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FEMORAL CENTERING SLEEVE

    FDA UDI
    Biomet Orthopedics, LLC·00880304254152·

    INTERLOCK FIBERED IDC OCCLUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SCIENT'X SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

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

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·October 6, 2016

    CAPSUREFIX MRI SURESCAN

    FDA Adverse Event
    Injury ·MPRI·Product code NVN·October 10, 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