38 results
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24ms
·
Sources: EU EUDAMED, US FDA
MICROBLADE SHAVER AND ACCESSORIES
FDA 510(k)
FDA Class 2
·Neurology
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA UDI
FX SOLUTIONS·03701037314975·Ø32 Eccentric Glenosphere with +3mm lateralized...
HMS NEUROMUSCULAR STIMULATOR, MODEL HMS 3
FDA 510(k)
FDA Class 2
·Neurology
AVID-NIT PLASTIC HUB LUTZ EPIDURAL NEEDLE,MODEL RP2035L, AVID-NIT METAL HUB LUTZ EPIDURAL NEEDLE, MODEL RM2035L
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
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·February 26, 2013