8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SUPER SCREW 3.5 MM
FDA 510(k)
FDA Class 2
·Orthopedic
BASE
FDA UDI
Nuvasive, Inc.·00887517701527·BASE HL Trial, 14x34x24mm 30°
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704285635·
TURBO-RAST SPECIFIC IGE ASSAY
FDA 510(k)
FDA Class 2
·Immunology
IS-2000 DIGITAL OPHTHALMIC IMAGING SYSTEM
FDA 510(k)
FDA Class 2
·Ophthalmic
CONSULTA CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·February 11, 2013
ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·December 13, 2010
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 24, 2014