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

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    RUSCH ENTERAL FEEDING TUBE

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

    OSSEOSPEED 4.0S-6MM, MODEL 24619

    FDA 510(k)
    FDA Class 2 ·Dental

    BANDAGE ROLL, GAUZE

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

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·June 21, 2019

    THERMOCOOL® SF BI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·February 15, 2013

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·July 29, 2014

    RHYTEC PORTRAIT PSR3

    FDA Adverse Event
    RHYTEC, INC.·Product code GEI·January 2, 2011

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·January 22, 2026