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

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    OPTION A02 MODEL 15202A

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MONDEAL

    FDA UDI
    MONDEAL Medical Systems GmbH·04050435061752·MCD Screw 3.0 x 24 mm M2 lockin...

    Lancer Gear

    FDA UDI
    LANCER ORTHODONTICS, INC.·00817573023875·HIGH-PULL"LANCER GEAR"BLACK/BLACK 5/PK

    CATALYST II AND III

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OLYMPUS FERRITIN REAGENT

    FDA 510(k)
    FDA Class 2 ·Immunology

    CX50 ULTRASOUND SYSTEM

    FDA Adverse Event
    Malfunction ·PHILIPS ULTRASOUND, INC·Product code IYN·April 2, 2024

    FIXED LANYARD 12" AND TP LIFT

    FDA Adverse Event
    Malfunction ·PRISM MEDICAL·Product code FSA·May 8, 2014

    RESOLUTION CLIP CLIPPING DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code MND·November 13, 2012

    ULTRA-THIN DIAMOND BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code LIT·September 10, 2010