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

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    WHITE RIVER MINI MANUAL BREAST PUMP

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    PEEK Corpectomy

    FDA UDI
    Nuvasive, Inc.·00887517623218·PEEK Corp Core, Ø12x31mm

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704293081·

    Endoform Topical Matrix

    FDA 510(k)
    FDA Unclassified ·Unknown

    EDAC QUANTIFIER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VACUETTE BLOOD COLLECTION TUBE 3ML K2E K2EDTA

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NA INC.·Product code JKA·November 2, 2020

    SPRINT FIDELIS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·January 26, 2011

    M2A-MAGNUM MOD HD SZ 52MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 31, 2014

    BIOSENSE WEBSTER NAVISTAR DS RMT DIAGNOSTIC/ABLATION STEERABLE CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC.·Product code LPB·September 7, 2007