6 results
·
35ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
NUFFIELD TOTAL KNEE
FDA 510(k)
FDA Class 2
·Orthopedic
GM501 Wash with Phenol Red and Gentamicin
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
RADAR VASCULAR COMPRESSION DEVICES
FDA 510(k)
FDA Class 2
·Cardiovascular
MEGA NEEDLE DRIVER INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·June 24, 2014
ASR 300 SPIKED CUP SIZE 62
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·November 3, 2010
HEARTSINE SAMARITAN 300P AND PAD PAK
FDA Adverse Event
Malfunction
·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·December 20, 2012