106 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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BOSTON ES (ENFLUFOCON A), BOSTON EO (ENFLUFOCON B) AND BOSTON XO (HEXAFOCON A) RIGID GAS PERMEABLE CONTACT LENSES
FDA 510(k)
FDA Class 2
·Ophthalmic
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00531241·
JOBST forMen
FDA UDI
BSN MEDICAL, INC.·04042809844979·FOR MEN 20-30 MM HG KNEE HIGH OPEN TOE LARGE FU...
NA
FDA UDI
Conmed Corporation·10845854018316·WIREDRIVER BRUSH
CANON X-RAY DIGITAL CAMERA WITH ADDITIONAL SOFTWARE, LANMIX MLT
FDA 510(k)
FDA Class 2
·Radiology
MODIFICATION TO SCOOPER DRUG/ADULTERATION TEST CUP
FDA 510(k)
FDA Class 2
·Clinical Toxicology
ENDOTRACH TUBE 8229507 CONTACT EMG 7MM
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC.·Product code ETN·January 7, 2014
NIM® 3.0 INTERFACE
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ETN·November 29, 2017
NIM® 3.0 MAINFRAME
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ETN·June 16, 2017
NIM® 3.0 MAINFRAME
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ETN·December 8, 2017
NIM® 3.0 MAINFRAME
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code GWF·August 30, 2016
MAINFRAME 8253001 NIM RESPONSE 3.0
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ETN·May 9, 2014
ENDOTRACHEAL TUBE 8229307 NIM EMG 7MM RE
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC.·Product code ETN·May 10, 2013
MAINFRAME 8253001 NIM RESPONSE 3.0
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC.·Product code ETN·May 8, 2013
NIM® 3.0 MAINFRAME
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ETN·March 23, 2017
NIM® 3.0 INTERFACE
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ETN·November 27, 2017
ENDOTRACHEAL TUBE 8229306 NIM EMG 6MM RE
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC.·Product code ETN·May 10, 2013
NIM® 3.0 MAINFRAME
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ETN·April 21, 2016
ZILVER 635 BILIARY SELF-EXPANDING STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·September 20, 2017
ZILVER 635 SELF-EXPANDING BILIARY STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·February 28, 2018