7 results
·
29ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
COLTENE A.R.T. BOND
FDA 510(k)
FDA Class 2
·Dental
Monster Screw System
FDA UDI
Paragon 28, Inc.·00889795120984·K-wire, Single Ended Trocar Tip, SMOOTH, 2.6 x ...
CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTOR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SYSTEM 1E Liquid Chemical Sterilant Processing System, SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6800, SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900, S40 Sterilant Concentrate
FDA 510(k)
FDA Class 2
·General Hospital
BIOFINITY TORIC COMFILCON A
FDA Adverse Event
Injury
·COOPERVISION MANUFACTURING LIMITED·Product code LPM·January 18, 2013
PIONEER PLUS CATHETER
FDA Adverse Event
Malfunction
·MEDTRONIC CARDIOVASCULAR·Product code DQY·November 12, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 14, 2014