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

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    PROD. NO. 01-132 - SUTURE REMOVAL KIT

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

    LPI ML210 HOLMIUM SURGICAL LASER, MODIFICATION

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

    RSVP SYSTEMS, SERIES I, BED-PATIENT MONITOR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·February 15, 2013

    LARGE SUTURECUT NEEDLE DRIVERINSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 29, 2014

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011