YY/T 1287.1-2016 Active Industry standards-Medicine

YY/T 1287.1-2016 Intracranial external drainage system—Part 1:Collecting sets for external drainage by intracranial puncture

YY/T 1287.1-2016 Intracranial external drainage system—Part 1:Collecting sets for external drainage by intracranial puncture

Publish Date: 2016-03-23 Implement Date: 2017-01-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: YY/T 1287.1-2016
Standard Type: Industry standards
Standard Status: Active
is_force_gb: no
CCS Name: Medical devices
ICS Name: Surgical implants, prostheses, and orthoses
Publish Date: 2016-03-23
Implement Date: 2017-01-01
Pages: 17 pages

Scope

This part of YY/T 1287 specifies the requirements for craniocerebral puncture external drainage collection devices in the craniocerebral external drainage system, and is applicable to cerebrospinal fluid ventricular external drainage and brain hemorrhage (or hematoma) external drainage.
The requirements for lumbar puncture external drainage devices, craniocerebral external drainage catheters, and intracranial pressure monitoring equipment are not within the scope of this part.

Development Information

Word Count: 28 Thousand words Pages: 17 pages

Same series standard

Referenced Standards

GB 8368-2005 Infusion sets for single use, gravity feed GB/T 17257.2-2009 Urine collection bags—Part 2:Requirements and test methods YY/T 0581.1-2011 Infusion access adapters—Part 1:Needle access adapters(Heparin plugs) YY/T 0581.2-2011 Infusion access adapter—Part 2:Needleless access adapters YY 0585.2-2005 Fluid lines for use with pressure infusion equipment and accessories for single use—Part 2:Accessories ISO 11607-1:2006 GB/T 1962.2-2001 Conical fittings with a 6%(Luer) taper for syringes, needles and certain other medical equipment—Part 2:Lock fittings 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 YY/T 1551.1-2017 Air filters for medical infusion and transfusion equipments—Part 1:Aerosol bacterial retention test method YY/T 1551.2-2017 Air filters for medical infusion and transfusion equipments—Part 2:Liquid bacterial retention test method YY/T 1551.3-2017 Air filters for medical infusion and transfusion equipments—Part 3:Integrity test methods

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