YY/T 1618-2018 Active Industry standards-Medicine

YY/T 1618-2018 Single-use needles for human venous blood specimen collection

YY/T 1618-2018 Single-use needles for human venous blood specimen collection

Publish Date: 2018-09-28 Implement Date: 2019-10-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: YY/T 1618-2018
Standard Type: Industry standards
Standard Status: Active
is_force_gb: no
CCS Name: Generally, it refers to microsurgical instruments
ICS Name: Blood transfusion, infusion, and injection equipment
Publish Date: 2018-09-28
Implement Date: 2019-10-01
Pages: 18 pages

Scope

This standard specifies the requirements for disposable human venous blood sample collection needles (hereinafter referred to as "collection needles") with a nominal outer diameter of 0.5 mm to 0.9 mm for venipuncture. This standard does not apply to the requirements for disposable human venous blood sample collection needles with visible blood return, but encourages manufacturers of disposable human venous blood sample collection needles with visible blood return to actively adopt the relevant provisions of this standard.

Development Information

Word Count: 32 Thousand words Pages: 18 pages

Referenced Standards

GB/T 14233.1-2008 Test methods for infusion,transfusion,injection equipments for medical use—Part 1:Chemical analysis methods GB/T 14233.2-2005 Test methods for infusion,transfusion,injection equipment for medical use—Part 2:Biological test methods GB/T 6682-1992 Water for analytical laboratory use—Specification and test methods GB/T 6682-2008 Water for analytical laboratory use—Specification and test methods GB 15810-2001 Sterile hypodermic syringes for single use GB 15810-2019 Sterile syringes for single use GB/T 16886.1-2001 Biological evaluation of medical devices—Part 1:Evaluation and testing GB/T 16886.1-2011 Biological evaluation of medical devices—Part 1:Evaluation and testing within a risk management process GB/T 16886.1-2022 Biological evaluation of medical devices—Part 1:Evaluation and testing within a risk management process GB 18279.1-2015 Sterilization of health care products—Ethylene oxide—Part 1:Requirements for development,validation and routine control of a sterilization process for medical devices GB 18280-2000 Sterilization of health care products—Requirement for validation and routine control—Radiation sterilization GB 18280.1-2015 Sterilization of health care products—Radiation—Part 1:Requirements for development,validation and routine control of a sterilization process for medical devices GB 18280.2-2015 Sterilization of health care products—Radiation—Part 2:Establishing the sterilization dose GB/T 18280.3-2015 Sterilization of health care products—Radiation—Part 3:Guidance on dosimetric aspects GB 18457-2001 Stainless steel needle tubing for manufacture of medical devices GB/T 18457-2015 Stainless steel needle tubing for the manufacture of medical devices GB/T 18457-2024 Stainless steel needle tubing for the manufacture of medical devices—Requirements and test methods YY/T 0296-1997 Hypodermic needles for single use—Colour coding for identification YY/T 0296-2013 Hypodermic needles for single use—Colour coding for identification YY/T 0296-2022 Hypodermic needles for single use—Colour coding for identification YY/T 0466.1-2009 Medical devices—Symbols to be used with medical device labels, labelling and information to be supplied—Part 1:General requirements YY/T 0466.1-2016 Medical devices—Symbols to be used with medical device labels,labelling and information to be supplied—Part 1:General requirements YY/T 0466.1-2023 Medical devices—Symbols to be used with information to be supplied by the manufacturer—Part 1:General requirements GB/T 18280.2-2025 Sterilization of health care products—Radiation—Part 2:Establishing the sterilization dose GB 18280.1-2025 Sterilization of health care products—Radiation—Part 1:Requirements for the development,validation and routine control of a sterilization process for medical devices GB/T 18280.3-2025 Sterilization of health care products—Radiation—Part 3:Guidance on dosimetric aspects of development,validation and routine control

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