BEUDAMED
    33 results · 25ms · Sources: EU EUDAMED, US FDA

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    Hercules Suture Anchor System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·00810116023288·270 Micron SU Thulio Performance 3m Fiber

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·00810116023264·200 Micron SU Thulio High Performance 3m Fiber

    Dornier Thulio Performance Fiber

    FDA UDI
    INNOVAQUARTZ LLC·00816959021870·

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·00810116023271·270 Micron SU Thulio Slim Performance 3m Fiber

    CODMAN

    FDA UDI
    Cerenovus, Inc.·10886704001386·CODMAN SLIM-LINE Aneurysm Clip 30 Degree Forwar...

    C-REACTIVE PROTEIN ANTISERUM KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    ALBUMIN REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 21, 2011

    FIREBIRD NXG

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code LXH·June 13, 2017

    TEXTURED SILICONE GEL GUMMY IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN·Product code FTR·April 2, 2020

    TENDRIL STS

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·January 13, 2014

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DTK·August 11, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 2, 2013

    GORE® ACUSEAL VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DSY·October 25, 2017

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Death ·W.L. GORE & ASSOCIATES·Product code MIH·March 23, 2017

    GORE® ACUSEAL VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DSY·October 25, 2017

    PIPELINE

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·October 20, 2019

    STIMULATOR, ELECTRICAL, IMPLANTABLE, FOR INCONTINENCE

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·October 26, 2016

    STIMULATOR, ELECTRICAL, IMPLANTABLE, FOR INCONTINENCE

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·October 26, 2016