91 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VENTRI 1.1
FDA 510(k)
FDA Class 2
·Radiology
Regent
FDA UDI
SPINAL ELEMENTS·00840916114794·Regent ACP 1-Level, 24mm
Slimplicity Anterior Cervical Plate System
FDA UDI
PRECISION SPINE, INC.·00815362021149·1 Level 24mm Plate
Symmetry Rhoton®
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482140208·Rhoton Bipolar Forceps; Bayonet; Titanium; 0.7 ...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450047514·
NA
FDA UDI
STRYKER CORPORATION·07613327052190·Bipolar Paddle Forceps with Spring Handle
SENSATION -VACUUM ASSIST DEVICES
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ARTHREX UNIVERS 30 SHOULDER PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
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