7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
MS CLASSIQUE BALLOON DILATATION CAHTETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BREATH ALCOHOL TEST SYSTEM, MODEL AL 2500
FDA 510(k)
FDA Class 1
·Clinical Toxicology
ETIII SA Fixture System (O3.2mm)
FDA 510(k)
FDA Class 2
·Dental
VERSYS FEMORAL STEM
FDA Adverse Event
Injury
·ZIMMER INC·Product code LPH·February 25, 2016
PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE
FDA Adverse Event
Malfunction
·MPRI·Product code LWP·February 9, 2013
FOLFUSOR SV 4ML/H
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·January 7, 2011
CORAIL2 LAT COXA VARA SIZE 9
FDA Adverse Event
Injury
·DEPUY FRANCE SAS 3003895575·Product code KWA·July 23, 2014