BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    OLSEN HEGAR NEEDLE HOLDERS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    STRADIS

    FDA UDI
    STRADIS MEDICAL, LLC·M75268212951·CUSTOM SURGICAL KIT VEIN PACK

    BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·August 9, 2021

    SAVIEW TORIC 55 (METHAFILCON A) SOFT (HYDROPHILIC) CONTACT LENSES FOR DAILY WEAR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ARTISTETM SOLUTION WITH SYS VCIO

    FDA 510(k)
    FDA Class 2 ·Radiology

    IMPLANT INSERTER

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code LXH·May 20, 2014

    PULSAR GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY LLC·Product code GEI·October 25, 2012

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Death ·W.L. GORE & ASSOCIATES·Product code MIH·August 26, 2010