35 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DELTACUT (APPARATUS AND CANNULA)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
RS NITRILSTST MEDICAL EXAMINATION GLOVES, POWDERED (NON STERILE) BLUE
FDA 510(k)
FDA Class 1
·General Hospital
EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
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
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code CBK·April 11, 2013
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 8, 2014