27 results
·
86ms
·
Sources: EU EUDAMED, US FDA
Tulip Medical Products, Inc.
FDA registration
Tulip Medical Products, Inc.·2 products·🇺🇸 United States
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·February 18, 2016
GUNTHER TULIP JUGULAR VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·November 24, 2017
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·February 10, 2017
GUNTHER TULIP JUGULAR VENA CAVA FILTER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code DTK·August 9, 2016
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·February 26, 2018
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code DTK·September 7, 2016
GUNTHER TULIP JUGULAR VENA CAVA FILTER SET
FDA Adverse Event
Malfunction
·WILLIAM COOK EUROPE·Product code DTK·March 2, 2017
GUNTHER TULIP JUGULAR VENA CAVA FILTER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code DTK·December 20, 2016
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·June 6, 2017
GUNTHER TULIP JUGULAR VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·December 15, 2016
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·May 9, 2016
UNKNOWN OPTEASE VENA CAVA FILTER
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code DTK·July 7, 2015
CORTERA SPINAL FIXATION SYSTEM
FDA Adverse Event
Malfunction
·XTANT MEDICAL HOLDINGS, INC.·Product code NKB·September 12, 2024
UNKNOWN
FDA Adverse Event
Injury
·COOK INC·Product code DTK·November 12, 2018
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·March 8, 2019
GUNTHER TULIP JUGULAR VENA CAVA FILTER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code DTK·July 6, 2017
HEMODIALYSIS BLOODLINES
FDA Adverse Event
Malfunction
·B. BRAUN MEDICAL INC.·Product code FJK·August 26, 2025
HEMODIALYSIS BLOODLINES
FDA Adverse Event
Malfunction
·B. BRAUN MEDICAL INC.·Product code FJK·August 26, 2025
HEMODIALYSIS BLOODLINES
FDA Adverse Event
Malfunction
·B. BRAUN MEDICAL INC.·Product code FJK·August 26, 2025