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JSA - JIS T 3233

Evacuated single-use containers for venous blood specimen collection

active, Most Current
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Organization: JSA
Publication Date: 29 July 2011
Status: active
ICS Code (Transfusion, infusion and injection equipment): 11.040.20

Document History

JIS T 3233
June 1, 2023
Evacuated single-use containers for human venous blood specimen collection
A description is not available for this item.
JIS T 3233
July 29, 2011
Evacuated single-use containers for venous blood specimen collection
A description is not available for this item.
JIS T 3233
March 25, 2005
Evacuated single-use containers for venous blood specimen collection
A description is not available for this item.

References

This document references:
ISO 17665-1 - Sterilization of health care products Moist heat Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by ISO on August 15, 2006
Inclusions This part of ISO 17665 specifies requirements for the development, validation and routine control of a moist heat sterilization process for medical devices. NOTE Although the scope of this...
This document references:
ISO TS 17665-2 - Sterilization of health care products — Moist heat — Part 2: Guidance on the application of ISO 17665-1
Published by ISO on January 15, 2009
This Technical Specification provides general guidance on the development, validation and routine control of moist heat sterilization processes and is intended to explain the requirements set forth...
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:
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:
ISO 11137-3 - Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects of development, validation and routine control
Published by ISO on June 1, 2017
This document gives guidance on meeting the requirements in ISO 11137-1 and ISO 11137-2 and in ISO/TS 13004 relating to dosimetry and its use in development, validation and routine control of a...
This document references:
ISO 11137-1 - Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices AMENDMENT 2: Revision to 4.3.4 and 11.2
Published by ISO on November 1, 2018
A description is not available for this item.
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