BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    MEDI-KLEER

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

    Swish™ Ball Abutment

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307115687·

    DEGUFILL (R) ADHESIVE

    FDA 510(k)
    FDA Class 2 ·Dental

    ALTERNATING PRESSURE PUMP AND PAD SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 17, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Malfunction ·Product code FKX·November 22, 2010

    ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·January 9, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 1, 2014

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021