16 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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XOMED-TREACE EMG ENDOTRACHEAL TUBEEN
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
ENDOTRACHEAL TUBE 7.5 MM EMG FLEX
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC.·Product code BTR·July 28, 2010
MAINFRAME 8253001 NIM RESPONSE 3.0
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC·Product code ETN·December 16, 2013
ENDOTRACH TUBE 8229306J NIM EMG 6MM
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED, INC·Product code ETN·March 6, 2013
ENDOTRACHEAL TUBE 8229307 NIM EMG 7MM RE
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC.·Product code ETN·May 10, 2013
ENDOTRACH TUBE 8229980 5PK 8MM EMG FLEX
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC.·Product code ETN·March 11, 2013
MAINFRAME 8253001 NIM RESPONSE 3.0
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED, INC.·Product code ETN·August 26, 2013
ENDOTRACH TUBE 8229980 5PK 8MM EMG FLEX
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED, INC.·Product code ETN·February 11, 2013
NIM® EMG - ENDOTRACHEAL TUBE - NIM FLEX¿
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code ETN·October 18, 2021
MAINFRAME 8253001 NIM RESPONSE 3.0
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED, INC.·Product code ETN·August 28, 2013
SOLID CORE GUTTA PERCHA CARRIER
FDA 510(k)
FDA Class 1
·Dental
VOYAGR SERIES OF DEFLECTABLE DIAGOSTIC EP CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
LARGE AO COUPLING ASNIS III HALL FITTING
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·September 25, 2012
RESTORE ULTRA
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LGW·January 22, 2013
CAPSURE Z NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010
SMALL PERIPHERAL CUTTING BALLOON®
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code LIT·July 10, 2014