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

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    IRIS G-PROBE

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

    IPV PERCUSSIONATOR FAMILY & RELATED ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    RENAFLO HDF 1350 HEMODIAFILTER

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

    BRAVO

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD.·Product code FFT·May 22, 2014

    STATAK SOFT TISSUE ATTACHMENT DEVICE DRIVER

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code MBI·November 2, 2010

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·December 20, 2012

    CIRCUIT PED 5FT DUAL-HTD 20/CS

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code BZE·June 1, 2012