BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Triathlon Total Knee System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MIO ADVANCE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code FPA·July 20, 2021

    NEW COMFORT-FIT DENTAL GUARD

    FDA 510(k)
    FDA Unclassified ·Unknown

    HQS INTRODUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ORIGEN BIOMEDICAL DUAL LUMEN 13FR CATHETER

    FDA Adverse Event
    Injury ·ORIGEN·Product code DWF·June 9, 2015

    PROMOTE PLUS CRT-D, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·October 15, 2014

    SYNREAM REAMING ROD Ø2.5 SHORT L950

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTO·June 17, 2013

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 24, 2011

    STOCKERT 70 RF GENERATOR

    FDA Adverse Event
    Injury ·STOCKERT GMBH·Product code DRF·February 22, 2011