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ASTM-F1830:2005 Edition

ASTM-F1830:2005 Edition

$35.75

F1830-97(2005) Standard Practice for Selection of Blood for in vitro Evaluation of Blood Pumps

Published By Publication Date Number of Pages
ASTM 2005 2
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1.1 This practice covers blood that will be used for in vitro performance assessments of blood pumps. These assessments include the hemolytic properties of the devices.

1.2 This practice covers the utilization of blood for the in vitro evaluation of the following devices:

1.2.1 Continuous flow rotary blood pumps (roller pumps, centrifugal pumps, axial flow pumps, and so forth) (see Practice F1841 ).

1.2.2 Pulsatile blood pumps (pneumatically driven, electromechanically driven, and so forth).

1.3 The source of blood utilized for in vitro evaluation of blood trauma (that is, hemolysis caused by the blood pumps, due to the pump design, construction, and materials used) substantially influences the results of the performance of these devices. Thus, a standardized blood source is required.

PDF Catalog

PDF Pages PDF Title
1 Scope
Referenced Documents
Terminology
Summary of Practice
Significance and Use
Collection and Preparation of Blood
2 Keywords
X1. CITRATE PHOSPHATE DEXTROSE ADENINE (CPDA1) SOLUTION USP
X1.1
X1.2
X2. HEPARIN
X2.1
X3. RATIONALE
X3.1

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