YY/T 1768.2-2021 Active Industry standards-Medicine

YY/T 1768.2-2021 Needle-based injection systems for medical use—Requirements and test methods—Part 2:Needles

YY/T 1768.2-2021 Needle-based injection systems for medical use—Requirements and test methods—Part 2:Needles

Publish Date: 2021-03-09 Implement Date: 2022-04-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: YY/T 1768.2-2021
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: 2021-03-09
Implement Date: 2022-04-01
Pages: 20 pages

Scope

YY/T 1768 This part specifies the requirements and test methods for disposable double-ended sterile needles.
This part is applicable to needles used with the needle injection system (NIS) specified in YY/T 1768.1.
This part is not applicable to dental needles, pre-filled injection needles, needles pre-assembled by manufacturers, or needles that do not require assembly or connection to the NIS.

Development Information

Word Count: 38 Thousand words Pages: 20 pages

Same series standard

Referenced Standards

GB/T 2423.4-2008 Environmental testing for electric and electronic products—Part 2:Test method—Test Db:Damp heat,cyclic(12 h+12 h cycle) 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 18457-2015 Stainless steel needle tubing for the manufacture of medical devices 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/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 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 YY/T 0615.1-2007 Requirements for medical devices to be designated "STERILE"—Part 1:Requirements for terminally sterilized medical devices

Adopt standards

ISO 11608-2:2012

Related Standards

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