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YY/T 1271-2016 English PDF

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YY/T 1271-2016: Cardiopulmonary bypass systems-Suction catheter for single use
Status: Valid

YY/T 1271: Evolution and historical versions

Standard ID	Contents [version]	USD	STEP2	[PDF] delivered in	Standard Title (Description)	Status	PDF
YY/T 1271-2016	English	199	Add to Cart	3 days [Need to translate]	Cardiopulmonary bypass systems-Suction catheter for single use	Valid	YY/T 1271-2016
YY/T 1271-2016	English	199	Add to Cart	3 days [Need to translate]	Cardiopulmonary bypass systems-Suction catheter for single use	Valid	YY/T 1271-2016

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Basic data

Standard ID	YY/T 1271-2016 (YY/T1271-2016)
Description (Translated English)	Cardiopulmonary bypass systems-Suction catheter for single use
Sector / Industry	Medical Device & Pharmaceutical Industry Standard (Recommended)
Classification of Chinese Standard	C45
Classification of International Standard	11.040.40
Word Count Estimation	9,935
Date of Issue	2016-03-23
Date of Implementation	2018-01-01
Issuing agency(ies)	State Food and Drug Administration
Summary	This standard specifies the classification, structure, requirements, test methods, signs, labels, instructions for use, packaging, transportation and storage of sterile disposable suction tubes (hereinafter referred to as suction tubes). This standard is applicable to the suction tube, which is used for supporting the cardiopulmonary bypass system. The suction tube is used for exhausting the left heart in cardiovascular surgery, suctioning decompression or reducing the load of the left heart, and sucking blood and other fluids in the cardiac surgery field.

YY/T 1271-2016: Cardiopulmonary bypass systems-Suction catheter for single use

---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
ICS 11:040:40 C45 Pharmaceutical Industry Standard of the People's Republic of China YY 1271-2016 cardiopulmonary bypass system Disposable suction tube According to the State Drug Administration medical device industry Standard Announcement (No: 76 of 2022), this standard is from From September 7, 2022, it will be converted into a recommended standard, no Enforce it again: 2016-03-23 release:2018-01-01 implementation Issued by China Food and Drug Administration

foreword

All technical contents of this standard are mandatory: This standard is drafted in accordance with the rules given in GB/T 1:1-2009: Please note that some contents of this document may refer to patents: The issuing agency of this document assumes no responsibility for identifying these patents: This standard was proposed by China Food and Drug Administration: This standard is under the jurisdiction of the National Standardization Technical Committee of Medical Extracorporeal Circulation Equipment (SAC/TC158): This standard was drafted by: Dongguan Kewei Medical Device Co:, Ltd:, State Food and Drug Administration Guangzhou Medical Device Quality Supervision and Inspection test center: The main drafters of this standard: Liu Yisheng, Tang Yunhua, Hong Liangtong, He Xiaofan: YY 1271-2016 cardiopulmonary bypass system Disposable suction tube

1 Scope

This standard specifies the classification, structure, requirements, test methods, signs, and labels of sterile single-use suction tubes (hereinafter referred to as suction tubes): label, instruction manual, packaging, transportation and storage: This standard is applicable to suction tubes for cardiopulmonary bypass systems, suction tubes for left heart exhaust, suction decompression or Reduce the load on the left heart and attract fluids such as blood in the cardiac surgery field:

2 Normative references

The following documents are indispensable for the application of this document: For dated references, only the dated version applies to this document pieces: For undated references, the latest version (including all amendments) applies to this document: GB/T 191-2008 Packaging, storage and transportation icon marks GB/T 9969-2008 General Rules for Instructions for Use of Industrial Products GB/T 14233:1-2008 Test methods for medical infusion, blood transfusion and injection equipment Part 1: Chemical analysis methods GB/T 14233:2-2005 Test methods for medical infusion, blood transfusion and injection equipment Part 2: Biological test methods GB/T 16886:1 Biological evaluation of medical devices Part 1: Evaluation and testing in the risk management process GB 18279 Medical Device Ethylene Oxide Sterilization Confirmation and Routine Control GB 18280 Sterilization Confirmation and Routine Control Requirements for Healthcare Products Radiation Sterilization GB 19335-2003 General technical requirements for disposable blood products YY/T 0149-2006 Test method for corrosion resistance of stainless steel medical devices YY/T 0466:1-2009 Symbols for medical device labeling, marking and providing information for medical devices Part 1: General Require YY/T 0681:1-2009 Test Methods for Sterile Medical Device Packaging Part 1: Guidelines for Accelerated Aging Tests

3 Classification and structure

3:1 Classification This standard stipulates that according to the use of the product, it is divided into two types: left heart drainage tube and cardiac suction tube (right heart suction tube); left heart drainage tube is mainly used for body In extracorporeal circulation heart surgery, it is used to exhaust the left heart, decompress or reduce the left heart load, and the heart cavity suction tube is mainly used in heart surgery with extracorporeal circulation: It is used to attract fluids such as blood in the cardiac surgery field, and transfer them back to the blood reservoir: The suction tube should be specified by the outer diameter or outer circumference of the product: Recommended in millimeters (mm), if not in millimeters (mm) place, the instruction manual should have a comparison table: The specific specifications, models and sizes are stipulated by the manufacturer according to its actual situation: YY 1271-2016

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