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YY 0285.3-2017 PDF English

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YY 0285.3-2017: [Including 2019XG1] Intravascular catheters - Sterile and single-use catheters - Part 3: Central venous catheters
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YY 0285.3: Evolution and historical versions

Standard IDContents [version]USDSTEP2[PDF] deliveryName of Chinese StandardStatus
YY 0285.3-2017English145 Add to Cart 0-9 seconds. Auto-delivery [Including 2019XG1] Intravascular catheters - Sterile and single-use catheters - Part 3: Central venous catheters Valid
YY 0285.3-1999English314 Add to Cart 3 days Sterile, single-use intravasoular catheters. Part 3: Central venous catheters Obsolete

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YY 0285.3-2017: [Including 2019XG1] Intravascular catheters - Sterile and single-use catheters - Part 3: Central venous catheters


---This is an excerpt. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.), auto-downloaded/delivered in 9 seconds, can be purchased online: https://www.ChineseStandard.net/PDF.aspx/YY0285.3-2017
YY PHARMACEUTICAL INDUSTRY STANDARD OF THE PEOPLE’S REPUBLIC OF CHINA ICS 11.040.20 C 31 Replacing YY 0285.3-1999 Intravascular catheters - Sterile and single-use catheters - Part 3. Central venous catheter (ISO 10555-3.2013, Intravascular catheters - Sterile and single-use catheters - Part 3. Central venous catheters, MOD) Issued on: JULY 17, 2017 Implemented on: SEPTEMBER 1, 2019 Issued by. China Food and Drug Administration

Table of Contents

Foreword ... 3 1 Scope ... 5 2 Normative references ... 5 3 Terms and definitions ... 5 4 Requirements ... 5

Foreword

YY 0285 "Intravascular catheters - Sterile and single-use catheters" consists of four parts. - Part 1. General requirements; - Part 3. Central venous catheters; - Part 4. Balloon dilatation catheters; - Part 5. Over-needle peripheral catheters. This Part is Part 3 of YY 0285. This Part was drafted in accordance with the rules given in GB/T 1.1-2009. This Part replaces YY 0285.3-1999 "Sterile single-use intravascular catheters - Part 3. Central venous catheters". Compared with YY 0285.3-1999, the main technical changes are as follows. - updated the normative references; - deleted Annex A. This Part uses redrafting method to modify and adopt ISO 10555-3.2013 "Intravascular catheters - Sterile and single-use catheters - Part 3. Central venous catheters". The technical differences and reasons between this Part and ISO 10555-3.2013 are as follows. - about normative references, this Standard made an adjustment on technical differences so as to adapt to the technical conditions in China; see Clause 2 "Normative references" for the adjustment, as follows. ● replaced ISO 10555-1.2013 with YY 0285.1-2017 that modified and adopted the International standard. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. The issuing authority shall not be held responsible for identifying any or all such patent rights. This Part was proposed by China Food and Drug Administration. This Part shall be under the jurisdiction of National Technical Committee on Medical Infusion Apparatus of China (SAC/TC 106). Intravascular catheters - Sterile and single-use catheters - Part 3. Central venous catheter

1 Scope

This Part specifies the requirements for sterile and single-use central venous catheter.

2 Normative references

The following referenced documents are indispensable for the application of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. YY 0285.1-2017, Intravascular catheters - Sterile and single-use catheters - Part 1. General requirements (ISO 10555-1.2013, MOD)

3 Terms and definitions

For the purposes of this document, the terms and definitions defined in YY 0285.1-2017 and the followings apply. 3.1 central venous catheter a central venous system is inserted for intravascular catheters for the delivery of fluids or blood samples and/or for pressure or other measurements, and is divided into single chambers or multiple chambers NOTE The catheter may have a fixation system as an integral part of the instrument.

4 Requirements

4.1 General The catheter shall comply with the requirements of YY 0285.1-2017 except for peak tension (see YY 0285.1-2017, 4.6). The peak tension shall meet the requirements of 4.4. 4.2 Distance mark ......
Source: Above contents are excerpted from the full-copy PDF -- translated/reviewed by: www.ChineseStandard.net / Wayne Zheng et al.