The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Dec. 29, 2014

Filed:

Jun. 09, 2004
Applicants:

Ronald O. Gilcher, Fort Myers, FL (US);

Jacques Chammas, Walpole, MA (US);

Joseph M. Medberry, Seekonk, MA (US);

Gary R. Stacey, Marshfield, MA (US);

Inventors:

Ronald O. Gilcher, Fort Myers, FL (US);

Jacques Chammas, Walpole, MA (US);

Joseph M. Medberry, Seekonk, MA (US);

Gary R. Stacey, Marshfield, MA (US);

Assignee:

Haemonetics Corporation, Braintree, MA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61M 31/00 (2005.12); G06Q 10/00 (2011.12); G06Q 50/00 (2011.12); G01N 33/48 (2005.12); G01N 33/50 (2005.12); A61B 5/00 (2005.12); B65D 81/00 (2005.12); A61M 1/00 (2005.12);
U.S. Cl.
CPC ...
Abstract

A whole blood collection system includes an automated pump/control unit and an accompanying disposable blood set. When combined and connected to a source of anticoagulant, these elements allow automatic priming of the blood set with anticoagulant and automatic collection of anticoagulated blood product according to three different collection modes. The unit's pump and the blood set are specially designed to cooperate during the collection process to assure that the collected product has a precise blood to anticoagulant ratio. During the collection procedure, the pump/control unit automatically collects data relating to the procedure. Additional data specifically identifying components of the blood set, such as the blood collection bag, along with identification data on the donor's registration form may be scanned into the pump/controller unit by a scanner associated with the unit; this facilitates positive sample identification and tracking. At the end of the procedure, a printer in the pump/controller unit automatically prints out this information so that a detailed record is immediately available about the collected blood product, the procedure for collecting it and the source of the product, i.e., the donor.


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