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JSA - JIS T 3217

Plastic collapsible containers for human blood and blood components

active, Most Current
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Organization: JSA
Publication Date: 1 October 2016
Status: active
ICS Code (Transfusion, infusion and injection equipment): 11.040.20

Document History

JIS T 3217
June 1, 2023
Plastic collapsible containers for human blood and blood components
A description is not available for this item.
JIS T 3217
October 1, 2016
Plastic collapsible containers for human blood and blood components
A description is not available for this item.
JIS T 3217
July 29, 2011
Plastic collapsible containers for human blood and blood components
A description is not available for this item.
JIS T 3217
March 25, 2005
Plastic collapsible containers for human blood and blood components
A description is not available for this item.

References

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 10993-11 - Biological evaluation of medical devices - Part 11: Tests for systemic toxicity
Published by ISO on September 1, 2017
This document specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.
This document references:
ISO 10993-12 - Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
Published by ISO on January 1, 2021
This document specifies requirements and gives guidance on the procedures in the preparation of samples and the selection of reference materials for medical device testing primarily in biological...
This document references:
ISO 10993-4 - Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood
Published by ISO on April 1, 2017
This document specifies general requirements for evaluating the interactions of medical devices with blood. It describes a) a classification of medical devices that are intended for use in contact...
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:
JIS T 0307 - Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied
Published by JSA on September 25, 2004
A description is not available for this item.
This document references:
JIS T 0993-1 - Biological evaluation of medical devices -- Part 1: Evaluation and testing within a risk management process
Published by JSA on January 1, 2020
A description is not available for this item.
This document references:
JIS T 3212 - Sterile blood transfusion set
Published by JSA on July 29, 2011
This Standard specifies the sterile blood transfusion sets for the transfusion of blood preparations such as preserved blood (hereafter referred to as "transfusion sets") that are ready to use and...
This document is referenced by:
JIS T 3212-4 - Sterile blood transfusion set - Part 4: Sterile transfusion sets for single use, gravity feed
Published by JSA on March 1, 2019
A description is not available for this item.
This document is referenced by:
JIS T 3212-5 - Sterile blood transfusion set - Part 5: Sterile transfusion sets for single use with pressure infusion apparatus
Published by JSA on March 1, 2019
A description is not available for this item.
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