9 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
GORE TAG THORACIC ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·May 14, 2021
CONFORMABLE GORE TAGTHORACIC ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·December 14, 2020
GORE® EXCLUDER®AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·June 27, 2022
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
CONFORMABLE GORE TAGTHORACIC ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·May 3, 2021
GORE TAG CONFORMABLE THORACIC STENT GRAFT WITH ACTIVE CONTROL SYSTEM
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·October 23, 2020