DIN EN ISO 6710:2017
Single-use containers for human venous blood specimen collection (ISO 6710:2017); German version EN ISO 6710:2017

Standard No.

DIN EN ISO 6710:2017

Release Date

2017

Published By

German Institute for Standardization

Status

Be replaced

Replace By

DIN EN ISO 6710:2017-12

Latest

DIN EN ISO 6710:2017-12

Replace

DIN EN 14820:2004 DIN EN ISO 6710:2016

Scope

This document specifies requirements and test methods for single-use receptacles, intended by their manufacturer, for the collection of venous blood specimens derived from the human body, for the purposes of in vitro diagnostic examination. This document also applies to receptacles containing media for blood culture.

DIN EN ISO 6710:2017 Referenced Document

• DIN EN ISO 11137-1:2015 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); German version EN ISO 11137-1:2015
• DIN EN ISO 11137-2:2015 Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2013); German version EN ISO 11137-2:2015
• DIN EN ISO 15223-1:2017 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2016, Corrected version 2017-03); German version EN ISO 15223-1:2016, with CD-ROM
• DIN EN ISO 17665-1:2006 Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006); English version of DIN EN ISO 17665-1:2006-11
• DIN ISO/TS 17665-2:2009 Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1 (ISO/TS 17665-2:2009); German version CEN ISO/TS 17665-2:2009
• EN 14820:2004 Single-use containers for human venous blood specimen collection
• EN 556-1:2001 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices*， 2024-04-20 Update
• EN 556-2:2015 "Sterilization of medical devices - Requirements for medical devices to be designated ""STERILE"" - Part 2: Requirements for aseptically processed medical devices"
• ISO 11137-1:2006 Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
• ISO 11137-2:2013 Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose
• ISO 15223-1:2016 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements
• ISO 17665-1:2006 Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
• ISO/TS 17665-2:2009 Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1

DIN EN ISO 6710:2017 history

• 2017 DIN EN ISO 6710:2017-12 Single-use containers for human venous blood specimen collection (ISO 6710:2017); German version EN ISO 6710:2017
• 2017 DIN EN ISO 6710:2017 Single-use containers for human venous blood specimen collection (ISO 6710:2017); German version EN ISO 6710:2017
• 1970 DIN EN ISO 6710 E:2016-11 Disposable containers for human venous blood sample collection (draft)
• 2016 DIN EN ISO 6710 E:2016 Draft Document - Single-use containers for venous blood specimen collection (ISO/DIS 6710:2016); German and English version prEN ISO 6710:2016
• 2004 DIN EN 14820:2004 Single-use containers for human venous blood specimen collection; German version EN 14820:2004
• 0000 DIN EN ISO 6710:2001
• 0000 DIN ISO 6710:1996

DIN EN ISO 6710:2017 Single-use containers for human venous blood specimen collection (ISO 6710:2017); German version EN ISO 6710:2017 has been changed from DIN EN 14820:2004 Single-use containers for human venous blood specimen collection; German version EN 14820:2004.