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

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    JULIET OL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Oticon

    FDA UDI
    Oticon A/S·05707131270245·H11, DESIGNRITE 10 WL CBE

    Fuji Cervical Plate System

    FDA UDI
    Altus Spine, LLC·B41711404741·74mm Level 4 Cervical Plate System - Fuji

    ACCUSOFT

    FDA 510(k)
    FDA Class 2 ·Radiology

    QUICKLASEDUAL+, QUICKLASE810, QUICKLASE810, QUICKLASE980, QUICKLASE980 MODEL: 3W,5W,3W,5W

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SJM MASTERS SERIES MECHANICAL HEART VALVE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL PUERTO RICO, INC.·Product code LWQ·July 6, 2016

    BD VIPER¿ LT SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code OOI·August 14, 2023

    PROMOS HUMERAL

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code HSD·May 31, 2013

    PROTECTIV SAFETY IV CATHETER

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL·Product code FOZ·June 23, 2011

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 3, 2014

    AVISTA MRI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 18, 2019