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

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    A-COMPANY ELASTIC ROTATION WEDGES

    FDA 510(k)
    FDA Class 1 ·Dental

    BREATHEX OMEGA CPAP DEVICE, MODEL 322

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ProteXsure Safety Capsule System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    EXTRACTION ROD, CONICAL T2 TIBIA Ø8 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·June 6, 2014

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·November 26, 2012

    PERFECTO2 V WITH SENSOR 9153650799

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·June 18, 2015

    2.7MM VA LCKNG SCREW SLF-TPNG WITH T8 STARDRIVE RECESS 36MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·June 21, 2016

    2.7MM VA LCKNG SCREW SLF-TPNG WITH T8 STARDRIVE RECESS 44MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·June 21, 2016

    2.7MM VA LCKNG SCREW SLF-TPNG WITH T8 STARDRIVE RECESS 40MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·June 21, 2016

    2.7MM VA LCKNG SCREW SLF-TPNG WITH T8 STARDRIVE RECESS 44MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·June 21, 2016

    2.7MM VA LCKNG SCREW SLF-TPNG WITH T8 STARDRIVE RECESS 30MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·June 21, 2016