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About This Item
Full Description
This document specifies requirements, including performance requirements, for plastics collapsible, non-vented, sterile containers (known as plastics containers) complete with collecting tube outlet port(s), integral needle, and with optional transfer tube(s), for the collection, storage, processing, transport, separation, and administration of blood and blood components. The plastics containers can contain anticoagulant and/or preservative solutions, depending on the application envisaged. This document is also applicable to multiple units of plastics containers, e.g. to double, triple, quadruple, or multiple units. Unless otherwise specified, all tests specified in this document apply to the plastics container as prepared ready for use. This document is not applicable to plastics containers with an integrated filter.
Document History
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DANSK DS/EN ISO 3826-1
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Plastics collapsible containers for human blood and blood components – Part 1: Conventional containers (ISO 3826-1:2019)- Most Recent
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DANSK DS/EN ISO 3826-1
Plastics collapsible containers for human blood and blood components – Part 1: Conventional containers- Historical Version
Amendments, rulings, supplements, and errata
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DANSK DS/EN ISO 3826-1/A1
Plastics collapsible containers for human blood and blood components – Part 1: Conventional containers – Amendment 1 (ISO 3826-1:2019/Amd1:2023) -
DANSK DSF/EN ISO 3826-1/PRA1
Plastics collapsible containers for human blood and blood components – Part 1: Conventional containers (ISO 3826-1:2019)