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16/30348158 DC : 0

Superseded
Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by
superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

BS EN ISO 6710 - SINGLE-USE CONTAINERS FOR VENOUS BLOOD SPECIMEN COLLECTION
Available format(s)

Hardcopy , PDF

Superseded date

10-31-2017

Language(s)

English

Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Materials
5 Draw volume
6 Design
7 Construction
8 Sterility and special microbiological states
9 Additives
10 Marking and labelling
11 Container identification
Annex A (normative) - Draw volume test
        for non-evacuated containers
Annex B (normative) - Draw volume test for
        evacuated containers
Annex C (normative) - Test for leakage of
        container
Annex D (normative) - Test for robustness
        of the container
Annex E (normative) - Concentrations of additives
        and volume of liquid additive
Annex F (informative) - Recommended colour code
        for identifying additives and accessories
Annex ZA (informative) - Relationship between
         this European standard and the essential
         requirements of Directive 98/79/EC
         [OJ L 331] aimed to be covered
Bibliography

BS EN ISO 6710.

Committee
CH/212
DocumentType
Draft
Pages
26
PublisherName
British Standards Institution
Status
Superseded
SupersededBy

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 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

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