8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
THE KEYMED HI-LIGHT 250 LIGHT SOURCE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Halyard
FDA UDI
O&M HALYARD, INC.·20680651686484·HALYARD,H600,STRWRP,-,48X48,48
ULTRA EXTERNAL CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MS-189 MUSCLE STIMULATOR
FDA 510(k)
FDA Class 2
·Physical Medicine
ATTAIN LDS LEFT-HEART DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code DQY·June 10, 2014
ENRHYTHM DR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code DXY·October 12, 2010
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 10, 2012
PLATE GC LECT AGAR 90MM 20
FDA Adverse Event
Malfunction
·BECTON DICKINSON GMBH·Product code JTY·March 29, 2021