BEUDAMED
    12 results · 23ms · Sources: EU EUDAMED, US FDA

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    ACE T4 REAGENT T4 CALIBRATORS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981377·anteriors; shade D2; mould US2

    NUVASIVE SURGICAL MESH SYSTEM

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

    PROSTEP MICA Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    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

    BD ULTRA-FINE PEN NEEDLES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMF·December 7, 2023

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 27, 2013

    COLD KNIFE, STRAIGHT BLADE, 3/PKG

    FDA Adverse Event
    Other ·GYRUS ACMI, INC·Product code GDX·February 3, 2011

    SENSOR ENLITE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZO·August 5, 2014

    AIRVANCE¿ THS SYSTEM - BONE SCREW WITH SUTURE

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

    AIRVANCE¿ THS SYSTEM - TOUNGE SUSPENSION KIT

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