10 results
·
29ms
·
Sources: EU EUDAMED, US FDA
PARKE-DAVIS NON-WOVEN SPONGE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
iNSitu™ Hip System
FDA UDI
NEXTSTEP ARTHROPEDIX, LLC·00816127028069·Neck Trial, Size 18, Standard, Dual Taper
PRIMA OXYGEN MONITOR
FDA 510(k)
FDA Class 2
·Anesthesiology
EXCELLAGEN
FDA 510(k)
FDA Unclassified
·Unknown
L.C. 5000/CE NITROGL
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·July 27, 2009
NITRO I.V. DC INF. SET W/LB TBG
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·May 16, 2011
L.C. 5000/CE NITROGLYCERIN PUM
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·February 22, 2012
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·January 9, 2014
PARADIGM INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code FRN·October 31, 2012
CARPENTIER-EDWARDS BIOPROSTHETIC VALVED CONDUIT
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·August 20, 2010