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ASTM-F1830:2017 Edition

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F1830-97(2017) Standard Practice for Selection of Blood for in vitro Evaluation of Blood Pumps

Published By Publication Date Number of Pages
ASTM 2017 3
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ASTM F1830-97-Reapproved2017

Historical Standard: Standard Practice for Selection of Blood for in vitro Evaluation of Blood Pumps

ASTM F1830

Scope

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.

1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.

1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

Keywords

blood trauma; condition of test blood; index of hemolysis; source of blood donor;

ICS Code

ICS Number Code 11.100 (Laboratory medicine)

DOI: 10.1520/F1830-97R17

ASTM-F1830
$35.75