FDA Clears Terumo BCT's PF24 and PF24RT24 Plasma Products
Published: Oct 08, 2012
FDA’s clearance of PF24 and PF24RT24 on the Trima Accel system is an opportunity to prepare plasma products from apheresis plasma collected at remote collection facilities and blood drives. Blood centers now have 24 hours before the product must be frozen.
PF24 and PF24RT24 plasma products are indicated for replacement of non-labile clotting factors. Clearance of PF24 and PF24RT24 has the potential to increase collection of plasma, and the availability of plasma from Type AB blood donors, the “universal donor” for plasma.
Mark Holmes, Vice President, Government and Regulatory Affairs
“FDA’s clearance of PF24 and PF24RT24 on the Trima Accel system enables customers to collect more plasma from mobile and satellite blood drives. Terumo BCT is excited about the greater collection options this presents customers, whether their collection site is one or many hours away. This increased time allowance before freezing has the potential to greatly increase plasma availability in the U.S., and help more patients, with the right product, at the right time.”
About Terumo BCT:
Terumo BCT, a global leader in blood component, therapeutic apheresis and cellular technologies, is the only company with the unique combination of apheresis collections, manual and automated whole blood processing, and pathogen reduction coupled with leading technologies in therapeutic apheresis and cell processing. We believe in the potential of blood to do even more for patients than it does today. This belief inspires our innovation and strengthens our collaboration with customers.
Laura Fusco, +1-303-205-2546
Global Corporate Communications