Active standard | Published: 15/08/2016

ISO 15676:2016-ed.2.0

Cardiovascular implants and artificial organs — Requirements for single-use tubing packs for cardiopulmonary bypass and extracorporeal membrane oxygenation (ECMO)
(Implants cardiovasculaires et organes artificiels — Exigences pour les paquets de tubes a usage unique pour pontage cardiopulmonaire et oxygénation des membranes extracorporelles)

Available languages: English

Available design: electronic design (pdf), Print design

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Detail information

Designation: ISO 15676:2016-ed.2.0

Publication date: 15/08/2016

Pages: 8

Country: International technical standard

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Anotation

Description / Abstract: 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.

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