DIN EN ISO 3826-3-2008
人体血液和血液成分用可折叠塑料容器.第3部分:带综合特征的采血袋系统(ISO 3826-3-2006)

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


DIN EN ISO 3826-3-2008 发布历史

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由德国标准化学会 DE-DIN 发布于 2008-03。

DIN EN ISO 3826-3-2008 在中国标准分类中归属于: C08 标志、包装、运输、贮存,在国际标准分类中归属于: 11.040.20 输血、输液和注射设备。

DIN EN ISO 3826-3-2008 发布之时,引用了标准

  • ISO 3826-1-2003 人类血液及血液成分用塑料折叠容器.第1部分:常规容器

DIN EN ISO 3826-3-2008的历代版本如下:

  • 2008年03月 DIN EN ISO 3826-3-2008 人体血液和血液成分用可折叠塑料容器.第3部分:带综合特征的采血袋系统(ISO 3826-3-2006)

 

 

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标准号
DIN EN ISO 3826-3-2008
发布日期
2008年03月
实施日期
废止日期
中国标准分类号
C08
国际标准分类号
11.040.20
发布单位
DE-DIN
引用标准
ISO 3826-1-2003
被代替标准
DIN EN ISO 3826-3-2007
适用范围
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系列标准


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