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BS ISO 17218:2014

Current

Current

The latest, up-to-date edition.

Sterile acupuncture needles for single use

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

31-05-2014

€271.12
Excluding VAT

Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Configuration
5 Requirements
6 Package
7 Labelling
8 Transit and storage
Annex A (informative) - Test methods for
        the intensity and sharpness of
        the tip of the needle
Annex B (informative) - Test methods for
        the puncture performance of
        the tip of the needle
Annex C (informative) - Test method for
        resistance to corrosion
Bibliography

Describes the requirements for the sterile acupuncture needles for single use (specialized for filiform needles).

Committee
CH/100/1
DevelopmentNote
Supersedes 13/30259011 DC. (05/2014)
DocumentType
Standard
Pages
36
PublisherName
British Standards Institution
Status
Current
Supersedes

This International Standard specifies the requirements for the sterile acupuncture needles for single use (specialized for filiform needles).

Standards Relationship
ISO 17218:2014 Identical

ISO 6507-1:2005 Metallic materials Vickers hardness test Part 1: Test method
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 10282:2014 Single-use sterile rubber surgical gloves — Specification
ISO 11607-2:2006 Packaging for terminally sterilized medical devices Part 2: Validation requirements for forming, sealing and assembly processes
ISO 6507-4:2005 Metallic materials Vickers hardness test Part 4: Tables of hardness values
ISO 15223-2:2010 Medical devices — Symbols to be used with medical device labels, labelling, and information to be supplied — Part 2: Symbol development, selection and validation
ISO 15510:2014 Stainless steels — Chemical composition
ISO 9626:2016 Stainless steel needle tubing for the manufacture of medical devices — Requirements and test methods
ISO 11737-2:2009 Sterilization of medical devices Microbiological methods Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
ISO 11737-1:2006 Sterilization of medical devices Microbiological methods Part 1: Determination of a population of microorganisms on products
ISO 6507-2:2005 Metallic materials Vickers hardness test Part 2: Verification and calibration of testing machines
2007/47/EC : 2007 COR 1 2015 DIRECTIVE 2007/47/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL OF 5 SEPTEMBER 2007 AMENDING COUNCIL DIRECTIVE 1990/385/EEC ON THE APPROXIMATION OF THE LAWS OF THE MEMBER STATES RELATING TO ACTIVE IMPLANTABLE MEDICAL DEVICES, COUNCIL DIRECTIVE 1993/42/EEC CONCERNING MEDICAL DEVICES AND DIRECTIVE 1998/8/EC CONCERNING THE PLACING OF BIOCIDAL PRODUCTS ON THE MARKET(TEXT WITH EEA RELEVANCE)
ISO 13485:2016 Medical devices Quality management systems Requirements for regulatory purposes
ISO 6507-3:2005 Metallic materials Vickers hardness test Part 3: Calibration of reference blocks
ISO 11138-2:2017 Sterilization of health care products — Biological indicators — Part 2: Biological indicators for ethylene oxide sterilization processes
ISO 11135-1:2007 Sterilization of health care products Ethylene oxide Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
EN 1041:2008+A1:2013 Information supplied by the manufacturer of medical devices
SAC GB 2024 : 1994 ACUPUNCTURE NEEDLES
ISO 10993-10:2010 Biological evaluation of medical devices Part 10: Tests for irritation and skin sensitization
ISO 780:2015 Packaging Distribution packaging Graphical symbols for handling and storage of packages
ISO 10993-11:2017 Biological evaluation of medical devices — Part 11: Tests for systemic toxicity
SAC GB/T 1031 : 1995 GEOMETRICAL PRODUCT SPECIFICATIONS (GPS) - SURFACE TEXTURE: PROFILE METHOD - SURFACE ROUGHNESS PARAMETERS AND THEIR VALUES
ISO 10993-7:2008 Biological evaluation of medical devices Part 7: Ethylene oxide sterilization residuals
ISO 11137-2:2013 Sterilization of health care products — Radiation — Part 2: Establishing the sterilization dose
ISO 7864:2016 Sterile hypodermic needles for single use — Requirements and test methods
ISO 10993-1:2009 Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
ISO 3696:1987 Water for analytical laboratory use — Specification and test methods
ISO 11138-1:2017 Sterilization of health care products — Biological indicators — Part 1: General requirements
ISO 14971:2007 Medical devices Application of risk management to medical devices
ISO 7000:2014 Graphical symbols for use on equipment Registered symbols
ISO 11607-1:2006 Packaging for terminally sterilized medical devices Part 1: Requirements for materials, sterile barrier systems and packaging systems
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 980:2008 Symbols for use in the labelling of medical devices
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
EN 10088-1:2014 Stainless steels - Part 1: List of stainless steels

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