9 results
·
25ms
·
Sources: EU EUDAMED, US FDA
TUBING CORRUGATED
FDA 510(k)
FDA Class 1
·Anesthesiology
CoRoent
FDA UDI
Nuvasive, Inc.·00887517360809·CoRoent SI Rasp, 11x17x14mm
discovery®
FDA UDI
DENTAURUM GmbH & Co.KG·J011790147000·discovery® Bracket with hook, - 7° Torque, 0° A...
COLOSSEUM Mesh
FDA 510(k)
FDA Class 2
·Orthopedic
BLOOD MONITORING UNIT, MODEL BMU 40
FDA 510(k)
FDA Class 2
·Cardiovascular
INSERT, BIPOLAR FORCEPS
FDA Adverse Event
Malfunction
·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code GEI·April 2, 2015
GUIDE
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code FZX·May 5, 2014
REVO MRI SURESCAN
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code LWP·October 15, 2012
TI MATRIXMANDIBLE LOCKING SCREW, SELF TAPPING
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code JEY·August 3, 2010