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

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    DIRECTIGEN GROUP A STREP TEST KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Lustre PRO Light System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Single Use RF Surgical Electrode (Needle Type) (AN-B, AN-C, AN-E, AN-I, AN-S, AN-W3A, AN-F3A, AN-IL, AN-SL, AN-W3B, AN-F1A, AN-F3B, AN-B3A)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·February 12, 2014

    MERIDIAN FILTER SYSTEM = FEMORAL

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·October 26, 2012

    PUMP MMT-715NAB PRDGM INS V2.1 BL EN

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code LZG·September 21, 2010