6 results
·
27ms
·
Sources: EU EUDAMED, US FDA
ELEVATOR
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
ARTHREX TENODESIS SCREW FAMILY
FDA 510(k)
FDA Class 2
·Orthopedic
ECHO TIP ULTRA FIDUCIAL NEEDLE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·May 30, 2014
RECEOVERY FILTER SYSTEM
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·October 23, 2012
LINOX SMART S 60
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code NVY·June 12, 2015