33 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SMARTmatic
FDA 510(k)
FDA Class 1
·Dental
LIFESHIELD LATEX-FREE GRAVITECH FLOW CONTROLLER I.V. SETS, MODELS 17528, 17527, 17525 & 17526
FDA 510(k)
FDA Class 2
·General Hospital
IRRIGATION SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
T:SLIM INSULIN DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code LZG·September 1, 2017
MICROBORE EXT SET
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code FPA·February 5, 2009
SOLUSET 100 BURETTE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·May 1, 2009
SOLUSET 100X60 CE-SL
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·June 18, 2009
SOLUSET 100X60 CE-SL
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·June 18, 2009
SOLUSET 150 BURETTE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·March 12, 2009
SOLUSET 100X60 CE-SL
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·June 18, 2009
SOLUSET 100X60 CE-SL
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·June 18, 2009
SVENTED IV PUMPSET/C
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·July 20, 2009
EXTENSION SET WITH T-CONNECTOR (500/CS)
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code FPA·March 25, 2010
EXTENSION SET WITH T-CONNECTOR (500/CS)
FDA Adverse Event
Malfunction
·HOSPIRA, LTD.·Product code FPA·March 25, 2010
EXTENSION SET WITH T-CONNECTOR (500/CS)
FDA Adverse Event
Malfunction
·HOSPIRA, LTD·Product code FPK·May 3, 2010
EXTENSION SET WITH T-CONNECTOR(500/CS)
FDA Adverse Event
Malfunction
·HOSPIRA, LTD.·Product code FPA·December 16, 2009
NV FIL SOLUSET 100
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA·Product code FPA·December 27, 2011
SOLUSET 100X60W/ CAI
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·July 19, 2013
NV FIL SOLUSET 100
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·July 22, 2010
ASR UNI FEMORAL IMPL SIZE 43
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·July 8, 2011