ISO 6710:2017
Current
The latest, up-to-date edition.
Single-use containers for human venous blood specimen collection
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25-07-2017
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ISO 6710:2017 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.
| DevelopmentNote |
Supersedes ISO 4822. (04/2001) Supersedes ISO/DIS 6710. (07/2017)
|
| DocumentType |
Standard
|
| Pages |
15
|
| PublisherName |
International Organization for Standardization
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| BS EN ISO 6710:2017 | Identical |
| NEN EN ISO 6710 : 2017 | Identical |
| SS-EN ISO 6710:2017 | Identical |
| PN EN ISO 6710 : 2018 | Identical |
| UNE-EN ISO 6710:2018 | Identical |
| UNI EN ISO 6710 : 2018 | Identical |
| DIN EN ISO 6710:2017-12 | Identical |
| SN EN ISO 6710 : 2018 | Identical |
| ONORM EN ISO 6710 : 2018 | Identical |
| IS 10867 : 2018 | Identical |
| I.S. EN ISO 6710:2017 | Identical |
| EN ISO 6710:2017 | Identical |
| GOST R ISO 6710 : 2009 | Identical |
| NF EN ISO 6710 : 2017 | Identical |
| GOST ISO 6710 : 2011 | Identical |
| BS ISO 6710:1995 | Identical |
| DIN ISO 6710:1996-12 | Identical |
| NS EN ISO 6710 : 2017 | Identical |
| 02/562438 DC : DRAFT MAY 2002 | PREN 14476 - CHEMICAL DISINFECTANTS AND ANTISEPTICS - VIRUCIDAL QUANTITATIVE SUSPENSION TEST FOR CHEMICAL DISINFECTANTS AND ANTISEPTICS USED IN HUMAN MEDICINE - TEST METHOD AND REQUIREMENTS (PHASE 2/STEP 1) |
| 02/564186 DC : DRAFT OCT 2002 | BS EN 14561 - CHEMICAL DISINFECTANTS - QUANTITATIVE CARRIER TEST FOR EVALUATION OF BACTERICIDAL ACTIVITY OF CHEMICAL DISINFECTANTS FOR INSTRUMENTS USED IN MEDICAL AREA - TEST METHOD AND REQUIREMENTS (PHASE 2/STEP 2) |
| 01/564180 DC : DRAFT OCT 2001 | BS EN 14254 - IN VITRO DIAGNOSTIC MEDICAL DEVICES - SINGLE-USE RECEPTACLES FOR THE COLLECTION OF SPECIMENS, OTHER THAN BLOOD, FROM HUMANS |
| 02/564188 DC : 0 | BS EN 14563 - CHEMICAL DISINFECTANTS - QUANTITATIVE CARRIER TEST FOR EVALUATION OF MYCOBACTERICIDAL ACTIVITY OF CHEMICAL DISINFECTANTS FOR INSTRUMENTS USED IN MEDICAL AREA - TEST METHOD AND REQUIREMENTS (PHASE 2/STEP 2) |
| EN 829 : 1996 | IN VITRO DIAGNOSTIC SYSTEMS - TRANSPORT PACKAGES FOR MEDICAL AND BIOLOGICAL SPECIMENS - REQUIREMENTS, TESTS |
| 02/564187 DC : DRAFT OCT 2002 | BS EN 14562 - CHEMICAL DISINFECTANTS - QUANTITATIVE CARRIER TEST FOR EVALUATION OF FUNGICIDAL ACTIVITY OF CHEMICAL DISINFECTANTS FOR INSTRUMENTS USED IN MEDICAL AREA - TEST METHOD AND REQUIREMENTS (PHASE 2/STEP 2) |
| 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 |
| 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/TS 17665-2:2009 | Sterilization of health care products — Moist heat — Part 2: Guidance on the application of ISO 17665-1 |
| 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 |
| EN 14820:2004 | Single-use containers for human venous blood specimen collection |
| 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 |
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