22 results
·
24ms
·
Sources: EU EUDAMED, US FDA
PhenoMATRIX
FDA 510(k)
FDA Class 2
·Microbiology
iFill
FDA UDI
Control Devices, LLC·G2982515110·Oxygen VIPR, IFILL, 0-10 L/min
Insignia
FDA UDI
ALPHATEC SPINE, INC.·00190376475332·Trial Drill Guide, 11mm
X SERIES
FDA UDI
Zoll Medical Corporation·00847946099534·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167312515110·
X SERIES
FDA UDI
Zoll Medical Corporation·00847946062552·X SERIES MONITOR/DEFIBRILLATOR 12 LEAD/W INTERP...
X SERIES
FDA UDI
Zoll Medical Corporation·00847946019754·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167322515110·
Reprocessed Endoscopic Trocars and Sleeves
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ROSA Spine
FDA 510(k)
FDA Class 2
·Neurology
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·January 11, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·January 11, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·March 13, 2019
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·September 3, 2014
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 16, 2011
FORCE FX
FDA Adverse Event
Malfunction
·COVIDIEN FORMERLY VALLEY LAB·Product code GEI·July 9, 2013
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·April 10, 2019
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code OLO·February 22, 2019
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code OLO·March 11, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·April 3, 2019