BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    TRANSFER PAK 4R 9006

    FDA 510(k)
    FDA Class 2 ·Hematology

    Power Dental USA

    FDA UDI
    Power Dental U.S.A. Inc.·D943781811·POWER TAC SCREW LARGE CASE BLUE 5mm X 10PCS (20...

    ReTrace Ureteral Access Sheath

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

    CARE3 PLUS

    FDA 510(k)
    FDA Class 1 ·Dental

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·November 23, 2017

    RIATA ST ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·April 30, 2014

    ANGLED DELIVERY DEVICE, GREENLIGHT XPS

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC.·Product code GEX·October 5, 2012

    UNIDENTIFIED ASR SLEEVE

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDG·May 19, 2015