GSO ASTM F1830:2022
Gulf Standard
Current Edition
·
Approved on
12 May 2022
·
Standard Practice for Collection and Preparation of Blood for Dynamic <emph type="bdit" >in vitro</emph> Evaluation of Hemolysis in Blood Pumps
GSO ASTM F1830:2022 Files
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GSO ASTM F1830:2022 Scope
1.1 This practice covers whole blood that will be used for
the in vitro performance assessment of hemolysis in blood
pumps intended for clinical use.
1.2 This practice covers the recommended standard
collection, preparation, handling, storage, and utilization of
whole blood for the in vitro evaluation (see Practice F1841) of
the following devices:
1.2.1 Continuous flow blood pumps (roller pumps, centrifugal pumps, axial flow pumps, etc.).
1.2.2 Pulsatile and intermittent flow blood pumps (pneumatically driven, electro-mechanically driven, with an artificial
pulse, etc.).
1.3 The source and preparation of whole blood utilized for
the dynamic in vitro evaluation of red blood cell (erythrocyte)
trauma caused by blood pumps can substantially influence the
hemolysis performance of these devices. Thus, standardized
whole blood collection and preparation methods are 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.
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