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

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    INTEGRATED DRIVE/PUMP SYSTEM FOR OTOLARYNGOLOGY

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981637·anteriors; shade D2 light; mould IL2

    LASER IMAGER DRYPRO MODEL 873

    FDA 510(k)
    FDA Class 2 ·Radiology

    DC-70/DC-70T/DC-70 Pro/DC-70 Exp/DC-75/DC-78/DC-70S Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    AIRVANCE BONE SCREW (REPOSE) SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code LRK·March 3, 2014

    AIRVANCE BONE SCREW (REPOSE) SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code LRK·March 29, 2013

    TAXUS® LIBERTÉ®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·February 27, 2013

    GUIDE WIRE HANDLE CHUCK 2-3, 5MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·January 12, 2011

    SUPER SUCKER SHORT (BX/20)

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code KDC·December 18, 2013

    AIRVANCE¿ THS SYSTEM - BONE SCREW WITH SUTURE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code LRK·November 30, 2015

    UMBILICAL CATHETER

    FDA Adverse Event
    Malfunction ·VYGON·Product code FOS·February 17, 2021

    AIRVANCE¿ THS SYSTEM - TOUNGE SUSPENSION KIT

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code LRK·October 2, 2015