7 results
·
22ms
·
Sources: EU EUDAMED, US FDA
HEMODIALYSIS VENOUS BLOOD TUBING SET OR SIMILAR TRADE NAME
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
FAMILI OF IRIDEX IQ LASER SYSTEMS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Relieva SpinPlus Nav Balloon Sinuplasty System
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·August 5, 2015
ACCU-CHEK ULTRAFLEX
FDA Adverse Event
Malfunction
·ROCHE HEALTH SOLUTIONS INC.·Product code FPA·January 30, 2013
DXTEND SCREW LOCK D4.5X30MM
FDA Adverse Event
Injury
·DEPUY FRANCE S.A.S.-SAINT PRIEST 3003895575·Product code KWS·July 31, 2014
IRIDEX IQ577 LASER SYSTEM
FDA Adverse Event
Injury
·IRIDEX CORP.·Product code GEX·November 4, 2013