7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
ELECTRODE, NEEDLE, CFM
FDA 510(k)
FDA Class 2
·Neurology
Sklar®
FDA UDI
SKLAR CORPORATION·10649111188152·JACKSON TUBE ORIG SHORT #1 STL
POWERPORT IMPLANTED PORT WITH GROSHONG CATHETER
FDA 510(k)
FDA Class 2
·General Hospital
Philips Hemodynamic Application R1.0
FDA 510(k)
FDA Class 2
·Cardiovascular
TRIDENT HEMISPHERICAL CLUSTER 54MM
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·April 30, 2014
CARPENTIER-EDWARDS PERIMOUNT RSR PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·October 10, 2012
PUMP MMT-522RNAS PRDGM INS SK EN RC
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code MDS·July 28, 2010