7 results
·
17ms
·
Sources: EU EUDAMED, US FDA
IN VITRO TEST DETERMINATION OF THEOPHYLLINE
FDA 510(k)
FDA Class 2
·Clinical Toxicology
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209128471·
MR Conditional Cup Electrodes
FDA 510(k)
FDA Class 2
·Neurology
H.R. JAKOBI SURG. INSTRUMENTS #11 25/39
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·June 6, 2014
AMS SPECTRA CONCEALABLE PENILE PROSTHESIS
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS, INC.·Product code FAE·November 29, 2012
TERUMO VIRTUOSAPH VEIN HARVESTING SYSTEM
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP·Product code GCJ·September 3, 2010