BEUDAMED
    6 results · 33ms · Sources: EU EUDAMED, US FDA

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    NEIVS TRACHEOTOMY RETRACTOR

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

    LAPAROSCOPE, FIBER LIGHT, PALMER-JACOBS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    PROWICK ANTIMICROBIAL POSTOPERATIVE WOUND DRESSING, SHOULDER AND KNEE, MODELS AR-1625, AR-1626

    FDA 510(k)
    FDA Unclassified ·Unknown

    XIRIS MEDICAL DEVICE DATA SYSTEM

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE ENTERPRISE IMAGING INFORMATICS·Product code LLZ·March 10, 2014

    RESTORE SENSOR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·October 4, 2012

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·July 28, 2010