14 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MEDRAD FLEX INTERFACE DEVICE
FDA 510(k)
FDA Class 2
·Radiology
F.A.S.T. 1
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·May 30, 2006
MODIFICATION TO SOLANAS POSTERIOR STABILIZATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ELAPSED TIME INDICATOR MODEL 21361A
FDA 510(k)
FDA Class 2
·Cardiovascular
FASTI INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009
COBAS 6000 E601 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LTJ·February 21, 2013
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVAMEX·Product code IOR·July 31, 2014
ELECSYS DIGOXIN
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code KXT·January 27, 2011