SS-EN-ISO-3826-1 › Historical Revision Information
Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers - Amendment 1

SS-EN-ISO-3826-1 - FOR 2019 EDITION AMENDMENT 1 SEE - CURRENT
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This part of ISO 3826 specifies requirements, including performance requirements, for plastics collapsible, non-vented, sterile 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 may contain anticoagulant and/or preservative solutions, depending on the application envisaged. This part of ISO 3826 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 part of ISO 3826 apply to the plastics container as prepared ready for use. This part of ISO 3826 is not applicable to plastics containers with an integrated filter.

To find similar documents by classification:

11.040.20 (Transfusion, infusion and injection equipment Including blood packs Syringes, needles and catheters, see 11.040.25)

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Designation Name

SS-EN ISO 3826-1:2004

Revision Level

FOR 2019 EDITION AMENDMENT 1 SEE

Status

Current

Publication Date

April 11, 2023

International Equivalent

EN ISO 3826-1:2003(IDT); ISO 3826-1:2003(IDT)