6 results
·
27ms
·
Sources: EU EUDAMED, US FDA
MAXILL-AIR SINUS VENTILATION TUBE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Carestream DRX-1 System with DRX Core Detectors
FDA 510(k)
FDA Class 2
·Radiology
1.5T GEM FLEX COIL
FDA 510(k)
FDA Class 2
·Radiology
FLEXI-SEAL SIGNAL FECAL MANAGEMENT SYSTEM KIT
FDA Adverse Event
Malfunction
·CONVATEC INC.·Product code KNT·March 31, 2014
CAPSURE Z NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD.·Product code MCM·August 24, 2010