8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
SCEPTORPETTE SYSTEM
FDA 510(k)
FDA Class 2
·Microbiology
COLLAR BUTTON VENT TUBE
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
MD212MC 21.3 DIAGNOSTIC IMAGING LCD MONITOR-L217TG
FDA 510(k)
FDA Class 2
·Radiology
COBAS 8000 C702 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·November 17, 2025
COBAS 8000 C702 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·February 27, 2026
OMNIPOD INSULIN PUMP
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code LZG·June 12, 2014
COOL-TIP RF SYS 100V ENG
FDA Adverse Event
Malfunction
·COVIDIEN LP (VALLEYLAB)·Product code GEI·October 22, 2010
DEPUY PINNACLE ACETABULAR CUP SYSTEM 56
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC·Product code KWA·December 17, 2012