8 results
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69ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TUBING SYSTEM FOR PLASMAPHERESIS
FDA UDI
KANEKA PHARMA AMERICA LLC·18855036020688·Indications for FH:
The Tubing System for Plasm...
TUBING SYSTEM FOR PLASMAPHERESIS
FDA UDI
KANEKA PHARMA AMERICA LLC·18855036012850·Indications for FH:
The Tubing System for Plasm...
SULFLUX
FDA UDI
KANEKA PHARMA AMERICA LLC·04537693900639·Indications for FH:
The SULFLUX KP-05 Plasma Se...
APHERESIS MACHINE
FDA UDI
KANEKA PHARMA AMERICA LLC·04987671040374·Indications for FH:
The Apheresis Machine KANEK...
XPRESS-WAY RX CATHETER,6F
FDA Adverse Event
Injury
·KANEKA PHARMA AMERICA LLC·Product code DXE·August 21, 2015
XPRESS-WAY RX CATHETER, 6FR
FDA Adverse Event
Injury
·KANEKA PHARMA AMERICA LLC·Product code DXE·January 13, 2017
XPRESS-WAY RX CATHETER, 6FR
FDA Adverse Event
Injury
·KANEKA PHARMA AMERICA LLC·Product code DXE·January 13, 2017
XPRESS-WAY RX CATHETER, 6FR
FDA Adverse Event
Injury
·KANEKA PHARMA AMERICA LLC·Product code DXE·January 13, 2017