12 results
·
29ms
·
Sources: EU EUDAMED, US FDA
BK-6453 RIMMED ACRYLIC LAP TRAY KIT
FDA 510(k)
FDA Class 1
·Physical Medicine
A-FIT®
FDA UDI
Gc Orthodontics America Inc.·E53581362700001·A-FIT® 1. MOLAR LWR LFT SZ 27
HEMASORB RESORBABLE HEMOSTATIC BONE PUTTY
FDA 510(k)
FDA Unclassified
·Unknown
SONOACE SA-8000 DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
ACTIVA
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code MHY·August 10, 2012
ACTIVA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·January 4, 2013
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·July 3, 2012
CLOSUREFAST CATHETER, 7F, 60CM
FDA Adverse Event
Malfunction
·COVIDIEN·Product code GEI·May 15, 2014
EXTERNAL PULSE GENERATOR
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA INC.·Product code DTE·October 31, 2012
ACRYSOF IQ TORIC
FDA Adverse Event
Other
·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·August 13, 2010
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·November 23, 2015
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·November 23, 2015