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

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    HISTOPLASMA CAPSULATUM, ANTIGEN

    FDA 510(k)
    FDA Class 2 ·Microbiology

    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

    Coblation

    FDA UDI
    Smith & Nephew, Inc.·00817470004472·PERC DLR SPINE WAND SURGICAL DEVICE

    SpineWand

    FDA UDI
    MORGAN STEER ORTHOPAEDICS LIMITED·05060696460002·Perc DLR Convenience Pack Inc 17 gauge 6” Crawf...

    NA

    FDA UDI
    aap Implantate AG·04042409174858·Direct measuring device L 270, CS 6.5-7.5, closed

    DIBS (Digital Indirect Bonding System)

    FDA 510(k)
    FDA Class 2 ·Dental

    COMFICARE PAD (FOR SINGEL PT USE)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BASIS

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWQ·October 16, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·December 31, 2013

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·May 18, 2015