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Evaluation of CPB devices relative to their capabilities of reducing the transmission of gaseous microemboli (GME) to a patient during cardiopulmonary bypass
Description
Evaluation of CPB devices relative to their capabilities of reducing the transmission of gaseous microemboli (GME) to a patient during cardiopulmonary bypass1 Scope This document recommends acceptable methodology for conducting gaseous microemboli (GME) testing and discusses limitations of current test methods. Tests described in this document are limited to those conducted using an in vitro circulatory system. This document is applicable to all devices intended for extracorporeal circulatory support during cardiopulmonary bypass (CPB). It outlines approaches currently used to assess the ability of CPB
PAS 2031 is used to ensure that the certification bodies which evaluate Energy Efficiency Measures installations against the requirements of PAS 2030 are doing so in a consistent and reliable way
The general information provided in BS EN ISO 14161 can have useful application for processes and biological indicators not currently addressed by existing standards
An E/E/PE safety-related system generally consists of sensors
cold chain
BS 6793 guidelines help manufacturers to streamline production so that users have access to superior products made from suitable materials
Priority pollutants have been defined by the EU and are listed in Council Decision 2455/2001/EC
Calculation method for source and sink temperature correction with fixed exergetic efficiency
as well as a range of ternary cements which include up to 20% limestone fines
The inclusion of all annexes of ISO 9001:2015 into ISO 15378:2017
nonutilitarian buttons are also used to enhance the appearance of the apparel
and intended-use alternatives
Helps in measuring the throw ratio
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