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

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    U-Motion II Acetabular System-Extension line

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VANGUARD SSK 360 REVISION KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AURORA DS

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

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·October 18, 2002

    GALILEO

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·November 20, 2008

    STELO GLUCOSE BIOSENSOR SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code SAF·August 13, 2025

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·November 3, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 24, 2011

    SERVO-I

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·July 3, 2013

    CAPTURE-R READY-SCREEN (3)

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·May 7, 2014