BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    BACTEC 9120 SYSTEM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    ZQUIET PRO-PLUS

    FDA 510(k)
    FDA Class 2 ·Dental

    MODIFICATION TO ARTHROCARE CONTROLLER (SYSTEM 2000 AND 8000), ARTHROCARE PATIENT CABLE, FOOT CONTROL, POWER CORD, WANDS

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

    NELLCOR OXIMAX N-65

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code DQA·June 2, 2014

    RESTORE

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 18, 2013

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010

    VARISOFT

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 26, 2024