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EN ISO 3826-3:2007 Standard

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  Keywords:

#requirements #part #specifies #specified #blood

  Directive

Medical devices Directive (93/42/EEC)

  Last Official Journal reference

Wednesday 14th of April 2021

  Description:

Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features (ISO 3826-3:2006)

  Purpose

This part of ISO 3826 specifies requirements, including performance requirements, for integrated features on plastic, collapsible, non-vented, sterile containers (blood bag systems). Blood bag systems need not contain all of the integrated features identified in this document. The integrated features refer to: - leucocyte filter; - pre-donation sampling device; - top-and-bottom bag; - platelet storage bag; - needle stick protection device. In addition to ISO 3826-1, which specifies the requirements of conventional containers, this part of ISO 3826 specifies additional requirements for blood bag systems using multiple units. This part of ISO 3826 does not cover automated blood collection systems. Unless otherwise specified, all tests specified in this part of ISO 3826 apply to the plastic container as prepared ready for use. Use chemical, physical and biological tests in accordance with ISO 3826-1, where applicable.

  Publication

Friday 17th of November 2017

  Related Standards

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EN 60627:2001/AC:2002

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EN 60645-2:1997

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EN 60645-3:2007

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Electroacoustics - Audiometric equipment - Part 3: Test signals of short durationIEC 60645-3:2007

EN 60645-4:1995

Medical devices Directive (93/42/EEC)

Audiometers - Part 4: Equipment for extended high-frequency audiometryIEC 60645-4:1994

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