BEUDAMED
    13 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    GLOBAL UNITE Platform Shoulder System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OLYMPUS INSTRUMENT TRAY

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SPEEDUP SOFTWARE OPTION

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code LKK·June 14, 2013

    GEM PREMIER 4000

    FDA Adverse Event
    Malfunction ·INSTRUMENTATION LABORATORY CO.·Product code CHL·June 22, 2011

    COLLEAGUE VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 24, 2008

    VASERLIPO SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code QPB·January 9, 2023

    GALAXY G3 MINI 1MM X 4CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·April 20, 2021

    GALAXY G3 MINI 1MM X 4CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·April 20, 2021

    GALAXY G3 MINI 2MM X 6CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·August 4, 2021

    GALAXY G3 MINI 1MM X 4CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·August 4, 2021

    GALAXY G3 MINI 1MM X 4CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·August 30, 2022

    SPIDER CERVICAL PLATING SYSTEM

    FDA Adverse Event
    Malfunction ·X-SPINE SYSTEMS, INC.·Product code KWQ·February 21, 2020