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

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    ATEC ALIF and LLIF Spacer System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MIRAGE FX

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ULTRA IABP CATHETER KIT, MODELS IMU7F-40, IMU7F-35, IMU7F-30, IMU7F-25, IMU7F-20

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 18, 2020

    6000CMS

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·June 11, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 8, 2011

    MINIMAL ACCESS ATTACHMENT

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBE·October 17, 2014