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DIN EN ISO 6710

Single-use containers for human venous blood specimen collection (ISO 6710:2017)

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Organization: DIN
Publication Date: 1 December 2017
Status: active
Page Count: 27
ICS Code (Transfusion, infusion and injection equipment): 11.040.20
scope:

This document specifies requirements and test methods for evacuated and non-evacuated single-use venous blood specimen containers.

It does not specify requirements for blood collection needles, needle holders, blood culture receptacles or "arterial" blood gas collection devices that can be used for venous blood.

Document History

DIN EN ISO 6710
December 1, 2017
Single-use containers for human venous blood specimen collection (ISO 6710:2017)
This document specifies requirements and test methods for evacuated and non-evacuated single-use venous blood specimen containers. It does not specify requirements for blood collection needles,...
DIN EN ISO 6710
November 1, 2016
Single-use containers for venous blood specimen collection (ISO/DIS 6710:2016); German and English version prEN ISO 6710:2016
A description is not available for this item.

References

This document references:
DIN EN 556-1 - Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices; English version of DIN EN 556-1
Published by DIN on March 1, 2002
A description is not available for this item.
This document references:
DIN EN 556-2 - Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices
Published by DIN on November 1, 2015
This European Standard specifies the requirements for an aseptically processed medical device to be designated 'STERILE'. NOTE For the purpose of the EU Directive(s) for medical devices (see...
This document references:
DIN EN 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 (ISO 11137-1:2006, including Amd.1:2013 + Amd.2:2018) (includes Amendment A2:2019)
Published by DIN on April 1, 2020
A description is not available for this item.
This document references:
DIN EN ISO 11137-2 - Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2013)
Published by DIN on November 1, 2015
This part of ISO 11137 specifies methods for determining the minimum dose needed to achieve a specified requirement for sterility and methods to substantiate the use of 25 kGy or 15 kGy as the...
This document is referenced by:
DIN EN 17111 - Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of virucidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)
Published by DIN on December 1, 2018
This document specifies a test method and the minimum requirements for virucidal activity of chemical disinfectant products that form a homogeneous, physically stable preparation when diluted with...
This document is referenced by:
DIN EN 17126 - Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of sporicidal activity of chemical disinfectants in the medical area - Test method and requirements (phase 2, step 1)
Published by DIN on February 1, 2019
This document specifies a test method and the minimum requirements for sporicidal activity of chemical disinfectant that form a homogeneous, physically stable preparation when diluted with hard...
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