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

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    CATHLAB SILICONE BILIARY BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    UCR

    FDA UDI
    Seaspine Orthopedics Corporation·10889981080211·RATCHETING DRIVER HANDLE

    POWER TILT AND RECLINE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    V-PRO 60 a Low Tempurature Strilization Systems, V-PRO s2 Low Temperature Sterilization Systems

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SILK SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAP·November 11, 2020

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·November 11, 2020

    QUATTRODE PERCUTANEOUS LEAD, 60 CM

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIV·Product code LGW·November 23, 2010

    INCEPTA

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 11, 2013

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    JIANGSU YUYUE MEDICAL EQUIPMENT & SUPPLY CO., LTD·Product code IKX·July 2, 2014

    ICAST COVERED STENT

    FDA Adverse Event
    Death ·ATRIUM MEDICAL CORPORATION·Product code JCT·March 18, 2021

    ICAST COVERED STENT

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORPORATION·Product code JCT·March 18, 2021