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

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    DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091982011·posteriors; shade A2; size L; lower jaw

    Integra Expandable Interbody

    FDA UDI
    Seaspine Orthopedics Corporation·10889981049430·Removal Tool. The Integra Expandable IBD System...

    SeaSpine Expandable Interbody

    FDA UDI
    Seaspine Orthopedics Corporation·10889981123659·Removal Tool

    PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MEDISTIM XP, TYPE 281 AND MEDITENS XP, TYPE 458

    FDA 510(k)
    FDA Class 2 ·Neurology

    UNKNOWN PARIETEX

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·June 26, 2019

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·May 18, 2015

    ASR UNI FEMORAL IMPL SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 28, 2013

    ACRYSOF IQ IOL 29.5 D

    FDA Adverse Event
    Malfunction ·ALCON LABORATORIES, INC.·Product code HQL·January 26, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 5, 2014

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 27, 2015