BEUDAMED
    10 results · 28ms · Sources: EU EUDAMED, US FDA

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    EXMOOR AURAL GROMMET

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Marienfeld Superior

    FDA UDI
    Paul Marienfeld GmbH & Co. KG·04250317350855·

    ORAGENE-DX OGD-500; ORAGENE-DX OGD-575; ORAGENE-DX OXD-525; ORAGENE-DX OYD-500

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MEDTRONIC SOFAMOR DANEK BIPHASIC CALCIUM PHOSPHATE (BCP) BONE VOID FILLER

    FDA 510(k)
    FDA Class 2 ·Dental

    GALAXY G3 MINI 1MM X 4CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·November 15, 2021

    LINER: VERSAFITCUP DM DOUBLE MOBILITY HC LINER 28/DMH

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·November 7, 2019

    LAMITRODE S8

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·April 28, 2014

    EXTERNAL PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DTE·October 31, 2012

    1644487-2008-00534

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·February 29, 2008

    Ingenia 3.0T CX-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Models: 781271

    FDA Enforcement
    Class II ·Completed·Philips North America Llc·September 15, 2021