BEUDAMED
    26 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GORE TAG THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·May 14, 2021

    COAPTITE

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC·Product code LNM·November 4, 2011

    CONFORMABLE GORE TAGTHORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·December 14, 2020

    COAPTITE

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LNM·November 4, 2011

    COAPTITE

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LNM·November 4, 2011

    COAPTITE

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LNM·November 4, 2011

    GORE® EXCLUDER®AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·June 27, 2022

    COAPTITE INJECTABLE IMPLANT

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC (FORMERLY BIOFORM MEDICAL, INC.)·Product code LNM·October 29, 2010

    COAPTITE

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LNM·November 4, 2011

    COAPTITE

    FDA Adverse Event
    Other ·MERZ AESTHETICS INC·Product code LNM·November 4, 2011

    COAPTITE INJECTABLE IMPLANT

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC (FORMALLY BIOFORM MEDICAL, INC)·Product code LNM·October 29, 2010

    COAPTITE INJECTABLE IMPLANT

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC. (FORMERLY BIOFORM MEDICAL, INC.)·Product code LNM·October 29, 2010

    COAPTITE

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC·Product code LNM·November 4, 2011

    COAPTITE

    FDA Adverse Event
    Other ·MERZ AESTHETICS INC·Product code LNM·November 4, 2011

    G7 SCREW 6.5MM X 25MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·July 28, 2017

    DUROM ACETABULAR COMPONENT 56/50 CODE P

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 3, 2013

    INTRATHECAL CATHETER

    FDA Adverse Event
    Injury ·RICE CREEK MANUFACTURING·Product code LKK·May 7, 2008

    PULSAR MAX II

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·April 5, 2011

    COAPTITE

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC·Product code LNM·November 4, 2011

    CONFORMABLE GORE TAGTHORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·May 3, 2021