28 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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6 FR POLY PER-Q-CATH TRIPLE LUMEN PICC
FDA 510(k)
FDA Class 2
·General Hospital
SIMPLICITY CLASSIC WING QD INFUSION SET
FDA 510(k)
FDA Class 2
·General Hospital
JEWEL CAST PLUS
FDA 510(k)
FDA Class 2
·Dental
UNKNOWN
FDA Adverse Event
Malfunction
·COOK, INC.·Product code DTK·August 21, 2014
UNK
FDA Adverse Event
Injury
·COOK, INC.·Product code DTK·August 20, 2014
UNKNOWN
FDA Adverse Event
Injury
·COOK INC·Product code DTK·August 20, 2014
IBP ELB INT. ULNA LRG RGT LNG STM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·June 24, 2016
MA204
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·April 9, 2013
OEM CAPIO SUTURES
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code MFJ·February 25, 2011
CONTAK RENEWAL 3 RF
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS, INC·Product code NIK·May 8, 2008
G7 VIVACIT-E 36MM I.D. SIZE E NEUTRAL LINER
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·August 19, 2024
GUNTHER TULIP VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·April 3, 2026
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·December 5, 2017
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code DTK·November 1, 2017
GUNTHER TULIP VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·November 4, 2025
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·February 27, 2018
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·May 5, 2017
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code DTK·May 12, 2017
UNKNOWN
FDA Adverse Event
Injury
·Product code DTK·August 20, 2020
UNK
FDA Adverse Event
Injury
·COOK, INC.·Product code DTK·August 20, 2014