BEUDAMED
    16 results · 17ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    2023337-1998-00001

    FDA Adverse Event
    Injury ·Product code FOA·December 22, 1998

    RINGLOC-X ARCOM LINER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·July 20, 2017

    RINGLOC-X E1 H/W 60/36MM 26

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·July 20, 2016

    1.5T SIGNA HDX ECHOSPEED

    FDA Adverse Event
    Injury ·GE MEDICAL SYSTEMS, LLC·Product code LNH·March 16, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·April 1, 2008

    RINGLOC-X E1 H/+3MM 50/36MM 23

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·February 1, 2016

    RINGLOC-X E1 H/W 60/36MM 26

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·July 20, 2016

    E1 HI-WALL LINER RINGLOC-X 60/36MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·March 7, 2017

    RINGLOC-X E1 10DEG 54/32MM 24

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·October 31, 2017

    E1 STANDARD +3MM LINER RINGLOC-X

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·May 18, 2017

    RINGLOC-X E1 H/W 58/36MM 25

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·March 24, 2017

    ARCOM XL HI-WALL LINER RINGLOC-X

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·September 7, 2017

    RINGLOC-X E1 STD

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·May 19, 2017

    RINGLOC-X E1 H/+3MM 50/36MM 23

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·December 18, 2015

    RINGLOC-X ARCOMXL STD 58/36MM 25

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·February 24, 2016

    E1 HI-WALL LINER RINGLOC-X 046MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·September 29, 2016