24 results · 19ms · Sources: EU EUDAMED, US FDA

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GLENOID, PE WITH PEG, SMALL

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code KWS·January 2, 2019

USP II HUMERAL HEAD 44/19

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code KWS·January 2, 2019

UNIVERS APEX HUMERAL STEM, 10MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code KWS·January 2, 2019

GLENOID, PE WITH PEG, SMALL

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code KWS·April 1, 2020

ARTHREX ECLIPSE HUMERAL HEAD, 41/16

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·December 4, 2019

ECLIPSE TRUNION,41 MM TPS CTD

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·December 4, 2019

ECLIPSE CAGE SCREW S, 30MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·December 4, 2019

GLENOID, PE WITH PEG, SMALL

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code KWS·August 7, 2024

UNIVERS VAULTLOCK GLENOID, SMALL

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code KWS·January 2, 2019

USP II HUMERAL HEAD 46/20

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code KWS·January 2, 2019

REPLY

FDA Adverse Event
Injury ·SORIN BIOMEDICA CRM S.R.L.·Product code NVZ·November 18, 2010

INGENIO

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 2, 2014

ARTHREX ECLIPSE HUMERAL HEAD, 43/16

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·November 16, 2020

ECLIPSE CAGE SCREW M, 35MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·November 16, 2020

ECLIPSE TRUNION,43 MM TPS CTD

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·November 16, 2020

GLENOID, PE WITH PEG, SMALL

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code KWS·December 4, 2019

GLENOID, PE WITH PEG, SMALL

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code KWS·December 5, 2022

ECLIPSE CAGE SCREW M, 35MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·April 9, 2021

ECLIPSE TRUNION,41 MM TPS CTD

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·April 9, 2021

UNIVERSAL APEX HUMERAL STEM, 6 MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code KWS·June 22, 2017