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

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    STERILIZATION INDICATOR FOR FLASH STERILIZATION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·14026704912473·

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704293821·

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771049965·Steinmann Pins, Single diamond, round end, 9/64...

    065 Zenith, 074 Zenith

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SENTEC DIGITAL MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    COBLATOR II

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code GEI·April 16, 2014

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·October 15, 2010

    PINNACLE MTL INS NEUT36IDX50OD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code KWA·December 13, 2012