7 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TWOFER NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
Ophthalmic Spatula
FDA UDI
KATENA PRODUCTS, INC.·00841668102527·ESCAF NUCLEUS MANIPULATOR
MULTICAM 3000 ECO
FDA 510(k)
FDA Class 2
·Radiology
BIOMARC TISSUE MARKER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PLUM A+ DRIVER NEW 8
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·February 10, 2014
STERIS SYSTEM 1E
FDA Adverse Event
STERIS CORPORATION - HOPKINS·Product code MED·November 14, 2012
KYPHX HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SPINE LLC·Product code NDN·September 3, 2010