BEUDAMED
    19 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    DELTA CER FEM HD 32/+3MM T1

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·July 21, 2016

    BIOLOX DELTA MODULAR CERAMIC HEAD 32MM STANDARD NECK TYPE 1 TAPER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·October 18, 2016

    BIOLOX DELTA MODULAR CERAMIC HEAD 32MM STANDARD NECK TYPE 1 TAPER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·October 18, 2016

    BIOLOX DELTA MODULAR CERAMIC HEAD 32MM STANDARD NECK TYPE 1 TAPER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·October 18, 2016

    DELTA CERAMIC FEM HD DIA36/ 0MM 12/14

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·August 2, 2016

    ALU FEM HD D28/+3.5/5 42/12-14

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LZO·June 17, 2016

    BIOLOX DELTA INSERT 36MM 54-56MM SHELL

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·June 22, 2016

    ALU FEM HEAD D32/0/5 42/12-14

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LZO·May 16, 2016

    ALU FEM HEAD D32/-4/5 42/12-14

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LZO·May 16, 2016

    ATTAIN STARFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·April 12, 2011

    G7 ACETABULAR LINER CERAMIC 32 MM F

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·January 8, 2016

    DELTA CER FEM HD 032/0MM 12/14

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·November 20, 2017

    BIOLOX DELTA OPTION HIP SYSTEM CERAMIC HEAD

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·September 15, 2016

    NANOTITE TM CERTAIN PREVAIL IMPLANT 4/5/4 X 15MM

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·December 4, 2023

    M2A-MAGNUM PF CUP 50ODX44ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 22, 2016

    M2A MAGNUM MODULAR HD COCR DIA 44MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 22, 2016

    BM ACET LP DOME SCW TI S/TAP D IA6.5X20MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 23, 2015

    E-POLY 36MM +3 MAXROM LNR SZ23

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MAY·December 23, 2015

    REGEN/RNGLC+ LTD 52MM SZ 23

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·December 23, 2015