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

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    RETRACTING PROBES

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172973998·UniTip High Resolution Catheter 8F

    RADIUS NEXT GENERATION GUIDEWIRE

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

    .DECIMAL ELECTRON APERTURE

    FDA 510(k)
    FDA Class 2 ·Radiology

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    GENTEEL HOMECARE PRODUCTS·Product code ITJ·May 15, 2014

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    LIGAMAX-5MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·August 23, 2010