836 results
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78ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BENTSON
FDA Adverse Event
Malfunction
·COOK, INC.·Product code DQX·May 21, 2015
Disposable Wire-Guided Scapel for Central Venous Cannulation
FDA UDI
SUNSET HEALTHCARE SOLUTIONS, INC.·00848530100162·Disposable Surgical Scalpel with Guide Channel ...
CLEANGUIDE
FDA Adverse Event
Malfunction
·CONMED CORPORATION·Product code OCY·May 9, 2023
EVOLUTION® ESOPHAGEAL CONTROLLED-RELEASE STENT - PARTIALLY COVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code ESW·December 3, 2020
VANTEX CENTRAL VENOUS CATHETER WITH OLIGON MATERIAL WITH OR WITHOUT AMC THROMBOS
FDA Adverse Event
Malfunction
·EDWARD LIFESCIENCES, PR·Product code DQO·May 30, 2008
ACROBAT® 2 CALIBRATED TIP WIRE GUIDE
FDA Adverse Event
Malfunction
·COOK ENDOSCOPY·Product code OCY·June 16, 2017
DISPOSABLE TWO-PART TROCAR NEEDLE
FDA Adverse Event
Injury
·COOK INC·Product code LJE·September 18, 2023
HIWIRE NITINOL HYDROPHILIC WIRE GUIDE
FDA Adverse Event
Injury
·COOK INC·Product code OCY·September 18, 2023
DISPOSABLE MARKED SPRING TIP GUIDEWIRE
FDA Adverse Event
Malfunction
·CONSOLIDATED MEDICAL EQUIPMENT COMPANY·Product code OCY·May 26, 2023
GUIDE WIRE, BALL-TIPPED, STERILE T2 TIBIA Ø3X800 MM
FDA Adverse Event
Injury
·STRYKER TRAUMA KIEL·Product code LXH·August 4, 2016
GUIDE WIRE, BALL-TIPPED, STERILE T2 HUMERUS Ø2.5X800 MM
FDA Adverse Event
Injury
·STRYKER TRAUMA KIEL·Product code LXH·April 25, 2016
FIELDER 18
FDA Adverse Event
Injury
·ASAHI INTECC CO., LTD.·Product code OCY·March 25, 2026
GUIDE WIRE, SMOOTH-TIPPED, STERILE T2 HUMERUS Ø2,2X800 MM
FDA Adverse Event
Injury
·STRYKER TRAUMA KIEL·Product code LXH·March 20, 2016
FIELDER 18
FDA Adverse Event
Injury
·ASAHI INTECC CO., LTD.·Product code OCY·October 1, 2025
CANNULATED DRILL 4.9MM FOR SCREWS 6.5MM LARGE AO
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS SELZACH·Product code HTW·August 27, 2009
PERIPHERAL CATHETER INSERTION KIT
FDA Adverse Event
Malfunction
·BARD ACCESS SYSTEMS, INC.·Product code OWL·October 2, 2017
ARROW/COOK
FDA Adverse Event
Injury
·ARROW/COOK·Product code GBP·July 24, 1992
PROSTAR XL SUTURE-MEDIATED CLOSURE
FDA Adverse Event
Injury
·AV-REDWOOD CITY·Product code MGB·November 22, 2010
DISPOSABLE MARKED SPRING TIP GUIDEWIRE
FDA Adverse Event
Malfunction
·CONSOLIDATED MEDICAL EQUIPMENT COMPANY·Product code OCY·May 26, 2023
AMPLATZ ULTRA STIFF PTFE FIXED CORE WIRE GUIDE
FDA Adverse Event
Malfunction
·COOK INC·Product code OCY·June 27, 2017