17 results
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37ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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THOMPSON MIS
FDA registration
THOMPSON MIS·6 products·🇺🇸 United States
Disposable BoneBac Press
FDA UDI
THOMPSON MIS·00858397006200·Disposable BoneBac Press - Single Use Box of 2
Disposable BoneBac Press
FDA UDI
THOMPSON MIS·00858397006217·Disposable BoneBac Press
Disposable BoneBac Press
FDA UDI
THOMPSON MIS·00858397006002·
AQUAMANTYS 6.0 BIPOLAR SEALER
FDA Adverse Event
Injury
·MEDTRONIC ADVANCED ENERGY, LLC·Product code DWG·September 12, 2013
AQUAMANTYS 6.0 BIPOLAR SEALER
FDA Adverse Event
Injury
·MEDTRONIC ADVANCED ENERGY, LLC·Product code DWG·September 12, 2013
AQUAMANTYS BIPOLAR SEALER (UNKNOWN)
FDA Adverse Event
Injury
·MEDTRONIC ADVANCED ENERGY, LLC·Product code DWG·July 30, 2013
TALENT TAA
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MIH·July 10, 2013
VALIANT
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MIH·July 10, 2013
TALENT AAA STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·December 13, 2017
TALENT AAA STENT GRAFT
FDA Adverse Event
Death
·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·December 13, 2017
TALENT AAA STENT GRAFT
FDA Adverse Event
Malfunction
·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·December 13, 2017
VALIANT
FDA Adverse Event
Death
·MEDTRONIC CARDIOVASCULAR·Product code MIH·April 3, 2014
TALENT TAA
FDA Adverse Event
Death
·MEDTRONIC CARDIOVASCULAR·Product code MIH·April 3, 2014
ECHELON FLEX 60 POWERED PLUS ENDOPATH STAPLER ARTICULATING ENDOSCOPIC LINEAR CUT
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 12, 2021
GORE® VIABAHN® ENDOPROSTHESIS WITH HEPARIN BIOACTIVE SURFACE
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code NIP·January 6, 2025
Xenon Diagnostic Circuit Kits labeled as "Xenon Diagnostic Circuit", "Xenon Circuit", and Needleless Xenon Diagnostic Circuit" Manufactured for RAF MEDICAL, INC., (Model number's RAF2306, RAF2304, RAF2380, RAF2300, RAF2370, RAF2372, RAF2350, RAF2341, RAF2302, RAF2340 RAF2306, RAF2304, RAF2361), or Medico-Mart, Inc. ("Xenon Curcuit" Model number's 2304, 2306). Xenon Diagnostic Circuit Kit: Used in specific Nuclear Medicine Procedures. ViroMax: For use on all patient populations, in conjunction with other respiratory devices containing standard 15 mm and/or 22 mm fittings (such as breathing circuits and the like) to filter respiratory gases where infection from airborne bacteria and viruses is a concern.
FDA Recall
Terminated
·Continental Medical Labs, Inc·Product code CAH·April 16, 2010