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Standard Practice for Selection of Blood for in vitro Evaluation of Blood Pumps
STANDARD published on 1.3.2013
Designation standards: ASTM F1830-97(2013)
Note: WITHDRAWN
Publication date standards: 1.3.2013
SKU: NS-51740
The number of pages: 3
Approximate weight : 9 g (0.02 lbs)
Country: American technical standard
Category: Technical standards ASTM
Keywords:
blood trauma, condition of test blood, index of hemolysis, source of blood donor, ICS Number Code 11.100 (Laboratory medicine)
Significance and Use | ||
5.1 The test results are substantially affected by donor species and age, the method of harvesting, the period of storage, the biochemical state of the blood, and the hemoglobin and hematocrit level of blood.5.2 Drawing several units of blood from healthy cattle does not affect them or their health. Therefore, bovine blood is strongly suggested for usage in experimental evaluation of blood damage. Mixing two donor sources of blood should be avoided in hemolysis tests because the mixture may induce added hemolysis or a change in red cell resistance against trauma. |
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1. 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 1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. |
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2. Referenced Documents | ||
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Historical
1.3.2013
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1.3.2010
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1.3.2011
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1.11.2009
Historical
1.12.2011
Historical
1.12.2011
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