14 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENT
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code FAD·June 8, 2023
VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENT
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code FAD·June 8, 2023
VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENT
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code FAD·June 8, 2023
VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENT
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code FAD·June 8, 2023
VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENT
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code FAD·June 8, 2023
VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENT
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code FAD·June 8, 2023
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code KWP·October 30, 2014
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·September 14, 2017
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·December 17, 2014
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·January 10, 2018
V40 COCR LFIT HEAD 36MM/+5
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·April 22, 2013
ARCHITECT TOTAL B-HCG
FDA Adverse Event
Malfunction
·A.I.D.D LONGFORD·Product code DHA·April 27, 2011
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 9, 2008
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·April 27, 2020