DIN EN ISO 3826-3:2008 PDF

Scope: 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.

DIN EN ISO 3826-3:2008 Referenced Document

ISO 3826-1:2003 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers

2008 DIN EN ISO 3826-3:2008-03 Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features (ISO 3826-3:2006); German version EN ISO 3826-3:2007
2008 DIN EN ISO 3826-3:2008 Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features (ISO 3826-3:2006); English version of DIN EN ISO 3826-3:2008-03
0000 DIN EN ISO 3826-3:2007