10 results
·
18ms
·
Sources: EU EUDAMED, US FDA
ESOPHAGEAL MOTILITY APPARATUS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
LEONE SPA
FDA UDI
LEONE SPA·08033707057031·DB TUBE MIM CONV 22 LEFT
LEONE SPA
FDA UDI
LEONE SPA·08033707063001·TUBE MIM CONV 22 LEFT
BoneCam
FDA UDI
MEDLINE INDUSTRIES, INC.·00818614021027·
BANDVIEW SYSTEM
FDA 510(k)
FDA Class 2
·Hematology
INTERLOCK-35 FIBERED IDC OCCLUSION SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·January 9, 2014
SPRINT FIDELIS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 31, 2012
SYNCRHOMED II
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·August 17, 2010
BD PHASEAL¿ INJECTOR LUER LOCK N35C
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code ONB·April 1, 2019