7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
EPINEED EPIDURAL CATHETER
FDA 510(k)
FDA Class 2
·Anesthesiology
MINS NEEDLESCOPIC RESPOSABLE DEVICE SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
AIRIS ELITE MAGNETIC RESONANCE IMAGING DEVICE
FDA 510(k)
FDA Class 2
·Radiology
80FRN
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·March 7, 2014
ARTHROSCOPE
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code HRX·November 14, 2012
ASAHI FIELDER XT PTCA GUIDE WIRE
FDA Adverse Event
Malfunction
·SETO FACTORY OF ASAHI INTECC CO., LTD., MEDICAL DIVISION·Product code DQX·September 3, 2010
8100 ALARIS PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·January 8, 2021