BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Lenstec LC Injection system

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    THREADED STEINMANN PINS, DOUBLE END BAYONET POINT

    FDA UDI
    Biomet Orthopedics, LLC·00887868016653·

    SCOUTPRO ACS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARTOURA BREAST TISSUE EXPANDER

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·March 31, 2020

    EVERA XT DR

    FDA Adverse Event
    Malfunction ·IPG MFG SWITZERLAND·Product code LWS·October 10, 2014

    CUSTOM HEMI SPOOL

    FDA Adverse Event
    Injury ·TORNIER INC·Product code HSD·June 6, 2013

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·July 14, 2011

    ARTOURA BREAST TISSUE EXPANDER

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·May 26, 2022

    ARTOURA BREAST TISSUE EXPANDER

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·October 10, 2020

    STARDRIVE SCREWDRIVER SHAFT T4/42MM/SELF-RETAINING

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HXX·January 28, 2019

    BD¿ NEXIVA SINGLE PORT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·March 21, 2019