BEUDAMED
    11 results · 29ms · Sources: EU EUDAMED, US FDA

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    UVB LIGHT BOX - UVB LIGHT BOOTH

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

    SpineWand

    FDA UDI
    MORGAN STEER ORTHOPAEDICS LIMITED·05060696460019·Perc DLG Convenience Pack inc 17 gauge 8” Crawf...

    Coblation

    FDA UDI
    Smith & Nephew, Inc.·00817470004489·PERC DLG

    Lacrimal Probe

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108734·BOWMAN LACRIMAL PROBE SET OF 6

    NA

    FDA UDI
    aap Implantate AG·04042409042102·Direct measuring device for K-Wire, L 250

    MODIFICATION TO PROFLU+ ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CALI·Product code FPA·May 6, 2014

    TRUETRACK

    FDA Adverse Event
    Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·April 29, 2015

    RELIA S

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NVZ·August 11, 2010

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018