BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    OHMEDA BAIN CIRCUIT ADAPTER GMS ABSOR

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    Buxton BioMedical

    FDA UDI
    Buxton Biomedical Inc·B7688434220·Sm-Hndl Punch, 230x2mm,40°up

    Prime Medical LLC

    FDA UDI
    Prime Medical LLC·00850055249288·PrimePadPlus-K14-3422

    SCALPEL

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

    ASAHI PTCA GUIDE WIRE, J SHAPE SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 2, 2014

    PEDIATRIC ULTRAMER CATHETER

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY KENDALL A DIVISION OF TYCO HEALTHCARE·Product code KOD·September 26, 2012

    COVIDIEN

    FDA Adverse Event
    Injury ·COVIDIEN·Product code MPB·September 22, 2010

    PM3544 QUADRA RELIEVE and PM3562 QUADRA ALLURE MP These low voltage (LV) devices are implantable pacemaker pulse generators, intended to be permanently implanted in the body, that have a power supply and electronic circuits that produce a periodic electrical pulse to stimulate the heart. These devices are used as a substitute for the heart's intrinsic pacing system to correct both intermittent and continuous cardiac rhythm disorders

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·October 25, 2017