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ASTM F 1830 : 1997 : R2013

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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

Available format(s)

PDF

Language(s)

English

Published date

01-03-2013

Superseded date

11-11-2014

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CONTAINED IN VOL. 13.01, 2017 Defines blood that will be used for in vitro performance assessments of blood pumps.

Committee
F 04
DocumentType
Standard Practice
Pages
3
ProductNote
Reconfirmed 2013
PublisherName
American Society for Testing and Materials
Status
Superseded
SupersededBy
Supersedes

1.1This practice covers blood that will be used for in vitro performance assessments of blood pumps. These assessments include the hemolytic properties of the devices.

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

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

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

1.3The 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.

1.4The 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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€60.83
Excluding VAT