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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    HYDRASORB(TM)

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

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756740401·ANGIOGRAPHY PACK

    IMPACTOR FOR FEMORAL HEAD

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    KINETIC MODEL 500

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

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT IRELAND·Product code CBK·May 21, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 12, 2010

    DIGITAL RADIOGRAPHY CXDI-70C WIRELESS

    FDA Adverse Event
    Malfunction ·CANON, INC.·Product code MQB·December 31, 2012