BEUDAMED
    251 results · 20ms · Sources: EU EUDAMED, US FDA

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    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·August 5, 2009

    PARAGON CRT

    FDA Adverse Event
    Other ·PARAGON VISION SCIENCES·Product code LPL·April 7, 2004

    JETSTREAM G3 SF

    FDA Adverse Event
    Other ·BAYER INTERVENTIONAL, INC.·Product code MCW·June 21, 2012

    3M ESPE FILETEK SUPREME PLUS FLOWABLE RESTOR

    FDA Adverse Event
    Other ·3M ESPE DENTAL PRODUCTS·Product code EBF·October 20, 2010

    SPECTRA CONCEALABLE PENILE PROSTHESIS

    FDA Adverse Event
    Other ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FAE·March 28, 2011

    3M ESPE ADPER SINGLE BOND PLUS ADHESIVE

    FDA Adverse Event
    Other ·3M ESPE DENTAL PRODUCTS·Product code KLE·December 9, 2010

    3M ESPE FILTEK SUPREME PLUS UNIVERSAL RESTO

    FDA Adverse Event
    Other ·3M ESPE DENTAL PRODUCTS·Product code EBF·December 9, 2010

    KARL STORZ

    FDA Adverse Event
    Other ·KARL STORZ GMBH & CO. KG·Product code KNS·June 7, 2012

    (BOVIE) HAND-TROL

    FDA Adverse Event
    Other ·CONMED CORP.·Product code GEI·April 6, 2000

    FORCEPS, 2MM GRASPING

    FDA Adverse Event
    Other ·CLARUS MEDICAL, LLC.·Product code HTD·September 22, 2004

    CRAGG-MCNAMARA VALVED INFUSION CATHETER

    FDA Adverse Event
    Other ·MICRO THERAPEUTICS, INC·Product code DQO·January 11, 2001

    HEARTSTART

    FDA Adverse Event
    Other ·LAERDAL MEDICAL A.S.·Product code MKJ·February 6, 2006

    BIRTCHER 4400

    FDA Adverse Event
    Other ·CONMED, CORP.·Product code GEI·August 5, 2008

    BARD

    FDA Adverse Event
    Other ·*·Product code KNW·September 13, 2005

    AESCULAP SET EJ701R, ED UR

    FDA Adverse Event
    Other ·AESCULAP, INC.·Product code GCJ·November 25, 1998

    ASPEN LABS EXCALIBUR ESU

    FDA Adverse Event
    Other ·ASPEN LABS·Product code GEI·August 22, 1997

    FEMORAL HEAD SYSTEM, 2MM

    FDA Adverse Event
    Other ·HOWMEDICA·Product code KWZ·July 3, 1995

    KARL STORZ

    FDA Adverse Event
    Other ·KARL STORZ GMBH & CO. KG·Product code GCJ·July 2, 2011

    3DKNEE

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code JWH·April 29, 2010

    LINVATEC

    FDA Adverse Event
    Other ·LINVATEC·Product code GEI·July 1, 1997