6,480 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Jay Adjustable Solid Seat
FDA UDI
SUNRISE MEDICAL (US) LLC·00016958040128·The Adjustable Solid Seat features ABS plastic ...
MONITOR DEFIBRILLATOR GPN
FDA Adverse Event
Death
·HEWLETT PACKARD·Product code DRK·July 13, 1993
FILIFORM DOUBLE PIGTAIL URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·May 22, 2023
SINGLE LUMEN POLYETHYLENE CENTRAL VENOUS CATHETER TRAY
FDA Adverse Event
Malfunction
·COOK INC·Product code FOZ·May 20, 2019
ACT ARTIC HD ARCOM XL 28X46MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWY·November 19, 2018
DELTA CERAMIC OPTION HEAD DIA2 8
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LZO·November 19, 2018
G7 PPS LTD ACET SHELL 58G
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PBI·October 10, 2018
DELTA CERAMIC FEMORAL HEAD Ø32/ 0MM T1
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·March 2, 2017
UNKNOWN
FDA Adverse Event
Injury
·COOK INC·Product code DYB·May 3, 2018
EVOLUTION DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code MUM·September 9, 2019
SAFE-T-J ROSEN CATHETER EXCHANGE WIRE GUIDE
FDA Adverse Event
Malfunction
·COOK INC·Product code DQY·December 13, 2017
UNKNOWN
FDA Adverse Event
Injury
·COOK INC·Product code DYG·May 8, 2018
UNKNOWN
FDA Adverse Event
Injury
·COOK INC·Product code DXE·May 9, 2018
COOK CELECT PLATINUM NAVALIGN FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·August 13, 2020
FLEXOR ANSEL GUIDING SHEATH
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·November 20, 2017
STENT, CORONARY
FDA Adverse Event
Death
·COOK INC·Product code MAF·June 9, 2022
UNKNOWN
FDA Adverse Event
Malfunction
·Product code LIT·October 29, 2018
STENT, CORONARY
FDA Adverse Event
Injury
·COOK INC·Product code MAF·June 9, 2022
BEACON TIP TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER
FDA Adverse Event
Death
·COOK INC·Product code DQO·April 8, 2020
1820334-2019-01090
FDA Adverse Event
Injury
·COOK INC·Product code BTR·May 16, 2019