UNLIMITED FREE
ACCESS TO THE WORLD'S BEST IDEAS

SUBMIT
Already a GlobalSpec user? Log in.

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

Customize Your GlobalSpec Experience

Select Your Free Newsletters

Industry Newsletters

Select Your Free Product Alerts

Finish!
Privacy Policy

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

DIN EN ISO 3826-1

Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2019)

active, Most Current
Buy Now
Organization: DIN
Publication Date: 1 January 2020
Status: active
Page Count: 32
ICS Code (Transfusion, infusion and injection equipment): 11.040.20

Document History

DIN EN ISO 3826-1/A1
July 1, 2022
Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers - Amendment 1 (ISO 3826-1:2019/DAM 1:2022); German and English version EN ISO 3826-1:2019/prA1:2022
A description is not available for this item.
DIN EN ISO 3826-1
January 1, 2020
Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2019)
A description is not available for this item.
DIN EN ISO 3826-1
April 1, 2018
Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO/DIS 3826-1:2018); German and English version prEN ISO 3826-1:2018
A description is not available for this item.
DIN EN ISO 3826-1
September 1, 2013
Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2013)
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...
DIN EN ISO 3826-1
April 1, 2004
Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2003)
A description is not available for this item.

References

This document references:
ISO 10993-5 - Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity
Published by ISO on June 1, 2009
This part of ISO 10993 describes test methods to assess the in vitro cytotoxicity of medical devices. These methods specify the incubation of cultured cells in contact with a device and/or extracts...
This document references:
ISO 3696 - Water for Analytical Laboratory Use - Specification and Test Methods
Published by ISO on April 15, 1987
Scope and field of application This International Standard specifies the requirements and corresponding test methods for three grades of water for laboratory use for the analysis of inorganic...
This document references:
10993-10 - Biological evaluation of medical devices — Part 10: Tests for skin sensitization
Published by ISO on November 1, 2021
This document specifies the procedure for the assessment of medical devices and their constituent materials with regard to their potential to induce skin sensitization. This document includes: —...
This document references:
ISO 3826-2 - Plastics collapsible containers for human blood and blood components — Part 2: Graphical symbols for use on labels and instruction leaflets
Published by ISO on August 1, 2008
This part of ISO 3826 addresses symbols that may be used to convey certain items of information related to medical devices dedicated to blood collection processes and storage. The information may be...
This document references:
ISO 3826-3 - Plastics collapsible containers for human blood and blood components Part 3: Blood bag systems with integrated features
Published by ISO on September 15, 2006
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...
View Less
View All
Advertisement