BEUDAMED
    7 results · 26ms · Sources: EU EUDAMED, US FDA

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    KODAK X-OMAT G FILM

    FDA 510(k)
    FDA Class 1 ·Radiology

    Delta Xtend Revers Shoulder System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HIVOX ELECTRIC STIMULATOR TENS & EMS, HD2

    FDA 510(k)
    FDA Class 2 ·Neurology

    MIDWEST LOW SPEED ATTACHMENTS - CONTRA ANGLE SHEATH

    FDA Adverse Event
    Malfunction ·SIRONA DENTAL SYSTEMS GMBH·Product code EFB·April 20, 2023

    PINNACLE MTL INS NEUT40IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·October 16, 2012

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 18, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2010