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

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    FlowTriever Retrieval/Aspiration System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EarQ

    FDA UDI
    Oticon A/S·05707131350435·G50 S, BTE PP 13 2.4G 105 C063 EARQ

    24M - Duke Energy FA/BBP

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588015149·24M - Duke Energy FA/BBP

    NEOGRAM PKU TANDEM MASS SPECTROMETRY KIT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MINICAM

    FDA 510(k)
    FDA Class 1 ·Dental

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 14, 2011

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 22, 2015

    HUDSON BACTERIAL/VIRAL FILTER

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CAH·February 8, 2016

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·October 17, 2008

    PLV-102

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·June 26, 2013

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·August 11, 2011

    ACRYSOF IQ TORIC SINGLEPIECE IOL

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. - HUNTINGTON·Product code MJP·May 22, 2015

    ACRYSOF IQ TORIC SINGLEPIECE IOL

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. - HUNTINGTON·Product code MJP·May 22, 2015

    ACRYSOF IQ TORIC SINGLEPIECE IOL

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. - HUNTINGTON·Product code MJP·May 22, 2015

    ACTIV.A.C. ION PROGRESS REMOTE THERAPY MONITORING SYSTEM

    FDA Adverse Event
    Injury ·KINETIC CONCEPTS, INC.·Product code OMP·June 8, 2021

    ACTIV.A.C. ION PROGRESS REMOTE THERAPY MONITORING SYSTEM

    FDA Adverse Event
    Injury ·KINETIC CONCEPTS, INC.·Product code OMP·July 14, 2021

    AS-OBGYN Information System version 7.824.x

    FDA Recall
    Terminated ·AS Software, Inc.·Product code LLZ·September 20, 2018

    ENDURANT II

    FDA Adverse Event
    Injury ·MEDTRONIC CARIOVASCULAR·Product code MIH·October 27, 2017

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·December 12, 2017

    SOFTEC HD

    FDA Adverse Event
    Injury ·LENSTEC BARBADOS INC.·Product code HQL·February 24, 2015