41 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AL ASKARI PERCUTANEOUS ACCESS NEEDLE HOLDER
FDA 510(k)
FDA Class 1
·Gastroenterology, Urology
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704282986·RETRACTOR MEYERDING MEDIUM 25 MILLIMETER X 70 ...
NAR Kit
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209101719·KIT, TACTICAL CRICKIT - CUSTOM
CUSA® Clarity Ultrasonic Surgical Aspirator System
FDA 510(k)
FDA Unclassified
·Unknown
GENEROS SB SMALL BONE DISTRACTION IMPLANT
FDA 510(k)
FDA Class 2
·Orthopedic
ZIMMON BILIARY STENT SET
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·October 25, 2018
ZIMMON BILIARY STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·August 14, 2018
ZIMMON BILIARY STENT SET
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·January 9, 2019
ZILVER 635 BILIARY SELF EXPANDING METAL STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·October 22, 2021
ZIMMON BILIARY STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·December 11, 2018
OASIS ONE ACTION STENT INTRODUCTION SYSTEM
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·December 11, 2018
COTTON-LEUNG BILIARY STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·September 4, 2020
COTTON-LEUNG BILIARY STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·September 4, 2020
COTTON-LEUNG BILIARY STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·September 4, 2020
COTTON-LEUNG BILIARY STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·September 4, 2020
COTTON-LEUNG BILIARY STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·September 4, 2020
COTTON-LEUNG BILIARY STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·August 16, 2018
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIQ·June 5, 2014
GORE HELEX SEPTAL OCCLUDER
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MLV·November 27, 2012
TRILOGY O2
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code CBK·June 17, 2015