BEUDAMED
    16 results · 23ms · Sources: EU EUDAMED, US FDA

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    FACTOR XII DEFICIENT PLASMA

    FDA 510(k)
    FDA Class 2 ·Hematology

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867050600·LO-PRO SCRW,TI,3.5MMX 34MM

    MODIFICATION TO CASPIAN SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Monarch Platform

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    AUTOPULSE® LI-ION BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code DRM·July 6, 2015

    IVT DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CALI·Product code KPE·January 2, 2013

    CLINITRON RITEHITE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC·Product code INX·February 14, 2014

    LOCKING SCREW, TITANIUM 3.5MM X 22MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 18, 2019

    LO-PRO SCRW,TI,3.5MMX 26MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 18, 2019

    LO-PRO SCRW,TI,3.5MMX 38MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 18, 2019

    LO-PRO SCRW,TI,3.5MMX 30MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 18, 2019

    CALCANEAL FRAC PERIMETER PLT,XS,RT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·April 18, 2019

    LO-PRO SCRW,TI,3.5MMX 24MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 18, 2019

    LO-PRO SCRW,TI,3.5MMX 34MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 18, 2019

    LO-PRO SCRW,TI,3.5MMX 36MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 18, 2019

    LOCKING SCREW, TITANIUM 3.5MM X 28MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 18, 2019