BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    MEICOR X-RAY TUBE, MODELS MC1000, MC1500, MC2000

    FDA 510(k)
    FDA Class 1 ·Radiology

    dentaform®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011882323220·dentaform® Band, tooth 16, size 23/Roth 22

    dentaform®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011882323180·dentaform® Band, tooth 16, size 23/Roth 18

    ARTHROCARE ARTHROWANDS

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

    PICO 7Y Single Use Negative Pressure Wound Therapy System

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

    ASR ACETABULAR CUPS 50

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·June 18, 2014

    MYNXGRIP VASCULAR CLOSURE DEVICE 6F/7F

    FDA Adverse Event
    Malfunction ·ACCESSCLOSURE, INC.·Product code MGB·December 20, 2012

    DELTEC COZMO INSULIN PUMP

    FDA Adverse Event
    Injury ·SMITHS MEDICAL MD (FORMERLY DELTEC, INC.)·Product code LZG·October 21, 2010