BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

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    ISOLAIR 2 FULL FACE SPLASH GUARD

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

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517396457·CoRoent® XLR, 12x38x28 15°

    VERRATA PRESSURE GUIDE WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Vyvo

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNSPECIFIED SAFESET TRANSPAC SETS

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·January 2, 2025

    REJUVENATE STRGHT PRFIT TMZF MOD STEM SIZE 8

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·January 28, 2013

    INOMAX DS (DELIVERY SYSTEM)

    FDA Adverse Event
    Malfunction ·INO THERAPEUTICS, LLC / IKARIA·Product code MRN·November 10, 2010

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·July 14, 2014