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ISO 15676:2016

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ISO 15676:2016

Cardiovascular implants and artificial organs — Requirements for single-use tubing packs for cardiopulmonary bypass and extracorporeal membrane oxygenation (ECMO)

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ISO 15676:2016 specifies requirements for single-use tubing packs for cardiopulmonary bypass and extracorporeal membrane oxygenation (ECMO). This document is applicable to all medical tubing intended for cardiopulmonary bypass (CPB) and/or extracorporeal membrane oxygenation (ECMO), but specific requirements and tests are included for tubing intended for use with peristaltic pumps during (short-term, i.e. <6 h duration) CPB surgery or (long-term, i.e. >24 h) ECMO procedures. The sterility and non-pyrogenicity provisions of this document are applicable to tubing packs labelled as 'sterile'.
It is applicable only to the tubing aspects for multifunctional systems that may have integral components such as blood gas exchangers (oxygenators), reservoirs, blood filters, defoamers, blood pumps, etc.

Author ISO/TC 150/SC 2 Cardiovascular implants and extracorporeal systems
Editor ISO
Document type Standard
Format Paper
Edition 2
ICS 11.040.40 : Implants for surgery, prosthetics and orthotics
Number of pages 8
Replace ISO 15676:2005
Weight(kg.) 0.1136
Year 2016
Country Switzerland