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

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    LIGHTWAVE INTEGRATED ELECTRODE ABLATOR AND LIGHT WAVE INTEGRATED ELECTRODE SUCTION ABLATOR

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

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517596796·CoRoent Large MP Ti, 9x9x23mm 4°

    KION ANAESTHESIA SYSTEM, MODEL 65 03 879 E392E

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BACT/ALERT PF CULTURE BOTTLE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    MAESTRO CARP PLATE 9X37 AUG 12

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWJ·March 14, 2016

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 10, 2013

    INSYNC MAXIMO

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·April 12, 2011

    DURATA STS OPTIM ACTIVE FIXATION LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008

    INTIMA-II Y 24GAX0.75IN PRN/EC SLM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 1, 2019

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·December 27, 2019

    MAESTRO RAD W/BRG 7X15 9.0 LT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KTT·December 17, 2015