15 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KTI TRANSPARENT WOUND DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
PHYSIO-DYNE EASI - LAB
FDA 510(k)
FDA Class 2
·Anesthesiology
SYSTEMATE ALBUMIN (EPOS APPLICATION) #65401
FDA 510(k)
FDA Class 2
·Clinical Chemistry
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
UNKNOWN WAGNER CONE PROSTHESIS HIP STEM
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·June 17, 2014
TRAUMA STRETCHER OBS 3/07
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FPO·January 22, 2013
SPRINT QUATTRO SECURE S
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 14, 2010
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