BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001

    FDA 510(k)
    FDA Class 1 ·Neurology

    PART 872 DEGUFILL H & DEGUFILL M DA

    FDA 510(k)
    FDA Class 1 ·Dental

    SURGICAL DISPOSABLE STERILE & NONSTERIL

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SYNCHRON® CK 2 X 400

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code CKA·May 10, 2011

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCORE·Product code CBK·January 11, 2013

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC·Product code LZG·December 3, 2010

    SENSOR ENLITE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZO·July 15, 2014