BEUDAMED
    179 results · 24ms · Sources: EU EUDAMED, US FDA

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    MAICO MA630D AUDIOMETER WITH OPTIONAL REFLEX DECAY & EUSTACHIAN TUBE FUNCTION

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    SIROLASER

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

    Balanced Knee System TriMax Porous Femoral Components

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    2953161-2010-00133

    FDA Adverse Event
    Injury ·July 8, 2010

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·August 31, 2006

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES·Product code MIH·August 27, 2013

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES, INC.·Product code MIH·June 4, 2007

    AORTIC EXCLUDER AAA ENDOPROSTHESIS (LOW PROFILE)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·March 22, 2019

    GORE INTRODUCER SHEATH

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES,INC·Product code DYB·January 3, 2008

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·May 8, 2014

    GORE TAG THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·August 12, 2011

    ABUT HEX-LOCK 4.5MM IMP 5 .5 FLARE

    FDA Adverse Event
    Malfunction ·ZIMMER DENTAL·Product code DZE·October 28, 2021

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·March 3, 2009

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·September 12, 2017

    ABUT GOLD FRICTION-FIT 3. 5MM IMP

    FDA Adverse Event
    Malfunction ·ZIMMER DENTAL·Product code DZE·April 3, 2018

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·February 9, 2013

    PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 7, 2011

    CURRENT DR RF

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·July 23, 2014

    GORE TAG THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES,INC·Product code MIH·September 21, 2011

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·October 21, 2021