45 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
HOSPIRA INFUSION BLOOD SETS
FDA 510(k)
FDA Class 2
·General Hospital
SOLUSET 100X60W/CAI
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·July 30, 2013
Y-SHAPED BLOOD SET W/ PUMP
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·September 12, 2013
Y-SHAPED BLOOD SET W/ PUMP
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code BRZ·September 13, 2013
SOLUSET 100X60W/CAI
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·August 6, 2013
SOLUSET 100X60W/CAI
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·December 17, 2013
NDEHP Y-BLOOD SET W/FILTER PUMP 203CM
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·February 24, 2011
SOLUSET 100X60W/CAI
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·August 6, 2013
SOLUSET 100X60W/CAI
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·December 10, 2013
SOLUSET 100X60
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·October 22, 2013
SOLUSET 100X60
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·October 22, 2013
SECONDARY SET CAIR CLAMP NON-DEHP
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·May 5, 2014
LIFESCHIELD PRIMARY SET CLAVE Y-SITE 100
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code FPA·July 21, 2014
LIFESHIELD PRIMARY SET CLAVE Y-SITE 100
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code FPA·July 21, 2014
PLUM SITE CHBR W/BALL PP YSTE 264CM NDHP
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·August 9, 2012
SECONDARY SET CAIR CLAMP NON-DEHP
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·May 5, 2014
PLUM SITE CHBR W/BALL PP YSTE 264CM NDHP
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·August 14, 2012
JOBST Bella Strong
FDA UDI
BSN MEDICAL, INC.·00035664012335·BELLA STRONG 20-30 MM HG GAUNTLET SIZE 1 NATURA...
Spine Wave Instruments
FDA UDI
Spine Wave, Inc.·10840642151190·Nerve Root Retractor, Long
BABY DOPPLEX 4000 (BD4000)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology