BEUDAMED
    52 results · 29ms · Sources: EU EUDAMED, US FDA

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    AFFINITY QS Q-SWITCHED ND:YAG LASER SYSTEM

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

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NQW·August 10, 2017

    100 SERIES OXYGEN ANALYZER, MODELS 1000-E AND 1000-I

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BLUE SENSOR, DISPOSABLE ECG ELECTRODES FOR ANAESTHESIA

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CENTERPIECE? PLATE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code NQW·April 16, 2015

    CENTERPIECE¿ PLATE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·June 8, 2016

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·December 7, 2017

    BD PHOENIX¿ SMIC-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·July 28, 2019

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·July 28, 2019

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NQW·May 22, 2019

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NQW·May 22, 2019

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·June 11, 2020

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NQW·March 1, 2018

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·February 22, 2018

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code OUT·April 10, 2013

    2017865-2008-01368

    FDA Adverse Event
    Malfunction ·Product code DXY·May 27, 2008

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·April 4, 2011

    FLUENCY PLUS TRACHEOBRONCHIAL STENT GRAFTS

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK·Product code JCT·May 22, 2009

    CENTERPIECE CONNECT PLATE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NQW·July 6, 2021