ISO 17218:2014
Current
The latest, up-to-date edition.
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English
03-02-2014
ISO 17218:2014 specifies the requirements for the sterile acupuncture needles for single use (specialized for filiform needles).
Committee |
ISO/TC 249
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DevelopmentNote |
Supersedes ISO/DIS 17218. (02/2014)
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DocumentType |
Standard
|
Pages |
24
|
ProductNote |
THIS STANDARD ALSO REFERS TO GB/DRT 2024-2010, KS P 3007:2009,YY 0043-2005,YY/T 0149-2006,YY 0666-2008,93/42/EEC,
|
PublisherName |
International Organization for Standardization
|
Status |
Current
|
Standards | Relationship |
BS ISO 17218:2014 | Identical |
AS ISO 17218:2014 | Identical |
NEN ISO 17218 : 2014 | Identical |
ISO/TR 20520:2018 | Traditional Chinese medicine Infection control for acupuncture treatment |
ISO 18746:2016 | Traditional Chinese medicine — Sterile intradermal acupuncture needles for single use |
15/30282343 DC : 0 | BS ISO 18746 - TRADITIONAL CHINESE MEDICINE - INTRADERMAL ACUPUNCTURE NEEDLES |
PD ISO/TS 16843-2:2015 | Health informatics. Categorial structures for representation of acupuncture Needling |
ISO/TS 16843-2:2015 | Health informatics — Categorial structures for representation of acupuncture — Part 2: Needling |
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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