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

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    DURACON STABILIZER FEMORAL COMPONENT AND INSERT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981202330·Interbody, 9mm x 32mm x 7mm, 0 deg

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981194345·Interbody, 9mm x 32mm x 7mm, 0 deg

    ELCACAM

    FDA 510(k)
    FDA Class 1 ·Dental

    VITA SUPRINITY(R)

    FDA 510(k)
    FDA Class 2 ·Dental

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·January 28, 2013

    SYNCHROMED EL

    FDA Adverse Event
    Malfunction ·RICE CREEK MANUFACTURING·Product code LKK·November 30, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 14, 2014

    BIOMET StageOne Knee Femoral Cement Spacer Mold, 70 MM, Silicone, Sterile, Item 432170.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020