11 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
0180 INTUITION, 0072 PRECISION
FDA 510(k)
FDA Class 2
·Radiology
BIODERM SCIENCES WOUND DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
NEUROLINK IP MODEL: PK1117
FDA 510(k)
FDA Class 2
·Neurology
ADMINISTRATION SET FOR HALO AMBULATORY INFUSION PUMP (TRADE NAME NIMBUS FLEX)
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FPA·November 21, 2018
ADMINISTRATION SET FOR HALO AMBULATORY INFUSION PUMP (TRADE NAME NIMBUS FLEX)
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FPA·November 21, 2018
ADMINISTRATION SET FOR HALO AMBULATORY INFUSION PUMP (TRADE NAME NIMBUS FLEX)
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FPA·November 21, 2018
ADMINISTRATION SET FOR HALO AMBULATORY INFUSION PUMP (TRADE NAME NIMBUS FLEX)
FDA Adverse Event
Malfunction
·INFUTRONIX LLC·Product code FPA·October 30, 2017
SYRINGE 0.5ML 29GA 12.7MM BLISTER 200BX
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·July 22, 2020
ARCHITECT CA 19-9XR
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code NIG·May 31, 2013
PAR 5 ACETABULAR SHELL
FDA Adverse Event
Other
·BIOMET, INC.·Product code JDI·July 24, 2008
*
FDA Adverse Event
Malfunction
·COVIDIEN·Product code GEI·June 9, 2011