6 results
·
27ms
·
Sources: EU EUDAMED, US FDA
IEC CENTRA-7 CENTRIFUGE MODEL 2362
FDA 510(k)
FDA Class 1
·Clinical Chemistry
CARDITTE MICROTEL
FDA 510(k)
FDA Class 2
·Cardiovascular
LENSES, EYEGLASS, SAFETY
FDA 510(k)
FDA Class 1
·Ophthalmic
NAIL, FIXATION, BONE
FDA Adverse Event
Malfunction
·SYNTHES(USA)·Product code JDS·April 30, 2014
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 27, 2007
ALARIS PUMP MODULE
FDA Adverse Event
Injury
·CAREFUSION CORP.·Product code FRN·October 3, 2012