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

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    SYNGO.VIA MI WORKFLOWS

    FDA 510(k)
    FDA Class 2 ·Radiology

    POWDER FREE LATEX EXAM GLOVES, POLY COATED NATURAL AND/OR COLORED, WITH PROTEIN LABELING (<50UN/G)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TRINON Q & Q3 IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    QUANTA SYSTEM S. P. A.

    FDA Adverse Event
    Malfunction ·QUANTA SYSTEM, S.P.A.·Product code GEX·December 9, 2014

    SOLITAIRE REVASCULARIZATION DEVICE

    FDA Adverse Event
    Injury ·COVIDIEN (IRVINE)·Product code NRY·April 24, 2015

    SOLITAIRE REVASCULARIZATION DEVICE

    FDA Adverse Event
    Death ·COVIDIEN (IRVINE)·Product code NRY·April 24, 2015

    MEDTRONIC MINIMED 670G

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code CGA·December 6, 2016

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 14, 2011

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 17, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·September 26, 2014