9 results
·
17ms
·
Sources: EU EUDAMED, US FDA
DYNACOR CONNECTING TUBING
FDA 510(k)
FDA Class 2
·General Hospital
Ophthalmic Spatula
FDA UDI
KATENA PRODUCTS, INC.·00841668102879·ROWEN DOUBLE ENDED PHACO SPATULA
ELECTROLY TE CHEMISTRY ANALYZER
FDA 510(k)
FDA Class 1
·Clinical Chemistry
PLUS PIVOT LINK UNIVERSAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
KATENA
FDA Adverse Event
Other
·Product code HND·February 26, 2009
2008K HEMODIALYSIS SYS. OLC/DIASAFE PLUS
FDA Adverse Event
Malfunction
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·March 27, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·November 14, 2012
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 10, 2015
Fortify, Sterile EO, Model #/ Part #: CD1231-40/100029238,100030095, 100041981; CD1231-40Q/100029229, 100030087, 100041982; CD1233-40/100029230, 100029250, 100029259,100031058, 100059778, 100070017; CD1233-40Q/100029260, 100029271, 100029277, 100031104, 100070089; CD1235-40/100029272, 100029282, 100029311, 100031039, 100059779; CD1235-40Q/100029273, 100029295, 100029312, 100030840; CD1241-40/100046351; CD1241-40Q/100046167; CD2231-40/100029274, 100030110, 100041922; CD2231-40Q/100029275, 100030089, 100041923; CD2233-40/100029147, 100029276, 100029313, 100031066, 100037043, 100048759, 100070007; CD2233-40Q/100029148, 100029263, 100029314, 100031067, 100037044, 100059770, 100070068; CD2235-40/100029149, 100029265, 100029283, 100031029, 100059837; CD2235-40Q/100029239, 100029258, 100029284, 100031030, 100066504; CD2241-40/100046148; CD2241-40Q/100046149; CD2299-40/100056952
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018