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ANSI/AAMI/ISO TIR19024:2016
Evaluation of CPB devices relative to their capabilities of reducing the transmission of gaseous microemboli (GME) to a patient during cardiopulmonary bypass
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Summary
This technical information report 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. Annex 3
Technical characteristics
| Publisher | Association for the Advancement of Medical Instrumentation (AAMI) |
| Publication Date | 01/01/2016 |
| Page Count | 0 |
| Themes | Implants & Artificial Organs |
| EAN | --- |
| ISBN | --- |
| Weight (in grams) | --- |
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