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YY 0117.2-2024 English PDF

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YY 0117.2-2024: Implants for surgery - Forgings, castings for bone joint prostheses - Part 2: ZTi6Al4V titanium alloy castings
Status: Valid

YY 0117.2: Historical versions

Standard IDUSDBUY PDFLead-DaysStandard Title (Description)Status
YY 0117.2-2024209 Add to Cart 3 days Implants for surgery - Forgings, castings for bone joint prostheses - Part 2: ZTi6Al4V titanium alloy castings Valid
YY 0117.2-2005110 Add to Cart Auto, < 3 mins Implants for surgery - Forgings, castings for bone joint prostheses - ZTi6A14V titanium alloy castings Valid
YY 0117.2-1993199 Add to Cart 2 days (Surgical implants of bone and joint prosthesis forging, casting alloy castings ZTiA16V4) Obsolete

Similar standards

YY 0118   YY/T 0119.1   YY/T 0119.4   YY 0117.3   YY 0117.1   

Basic data

Standard ID: YY 0117.2-2024 (YY0117.2-2024)
Description (Translated English): Implants for surgery - Forgings, castings for bone joint prostheses - Part 2: ZTi6Al4V titanium alloy castings
Sector / Industry: Medical Device & Pharmaceutical Industry Standard
Classification of Chinese Standard: C35
Classification of International Standard: 11.040.40
Word Count Estimation: 10,146
Date of Issue: 2024-07-08
Date of Implementation: 2027-07-20
Older Standard (superseded by this standard): YY 0117.2-2005
Issuing agency(ies): State Drug Administration

YY 0117.2-2024: Implants for surgery - Forgings, castings for bone joint prostheses - Part 2: ZTi6Al4V titanium alloy castings


---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 CCSC35 Pharmaceutical Industry Standards of the People's Republic of China Replaces YY 0117.2-2005 Surgical implants, bone and joint prostheses, forgings and castings Part 2.ZTi6Al4V titanium alloy castings Released on 2024-07-08 2027-07-20 Implementation The State Drug Administration issued

Foreword

This document is in accordance with the provisions of GB/T 1.1-2020 "Guidelines for standardization work Part 1.Structure and drafting rules for standardization documents" Drafting. This document is part 2 of YY 0117 "Surgical Implants - Bone and Joint Prosthesis Forgings and Castings". YY 0117 has been issued as follows part. --- Part 1.Ti6Al4V titanium alloy forgings; --- Part 2.ZTi6Al4V titanium alloy castings; --- Part 3.Cobalt-chromium-molybdenum alloy castings. This document replaces YY 0117.2-2005 "Surgical Implant Bone and Joint Prosthesis Forgings and Castings ZTi6A14V Titanium Alloy Castings" and Compared with YY 0117.2-2005, in addition to structural adjustments and editorial changes, the main technical changes are as follows. --- Deleted the requirements for casting process (see 3.4 of the.2005 edition); --- Changed the internal quality requirements. The allowable level of internal defects can meet the requirements of both the supplier and the buyer in accordance with the Appendix of YY/T 1565-2017. A recommended acceptable limit agreed limit (see 4.5, 3.7 of the.2005 edition); --- Changed the test method for chemical composition analysis and added other recognized analysis methods (existing ISO methods or national standards, industry standards, etc.) Methods recommended by industry standards) (see 5.1, 4.1 of the.2005 edition); --- Added test methods for surface contamination (see 5.3.1); --- Changed the test method for surface roughness. In addition to the sample comparison method, the test method of GB/T 10610 was added (see 5.3.3, 4.5 of the.2005 edition); --- Changed the test method for surface quality, added magnifying glass and fluorescent penetrant inspection methods (see 5.3.4, 4.5 of the.2005 edition). Please note that some of the contents of this document may involve patents. The issuing organization of this document does not assume the responsibility for identifying patents. This document is proposed by the State Food and Drug Administration. This document is under the jurisdiction of the National Technical Committee for Standardization of Surgical Implants and Orthopedic Devices (SAC/TC110). This document was drafted by. Beijing Youcai Jinghang Biotechnology Co., Ltd., Tianjin Medical Device Quality Supervision and Inspection Center, National Drug Administration Medical Device Technical Review Center of the State Food and Drug Administration, Greater Bay Area Center for Medical Device Technical Review and Inspection of the State Food and Drug Administration, Beijing Chunli Zhengda Medical Equipment Co., Ltd. The main drafters of this document are. Xiong Zhenguo, Qin Geji, Liu Dacheng, Fu Ruizhi, Zhu Jinqing, Sun Jiayi, Wu Jing, Zhang Yidan, Li Niya, Lu Minqi, Zhang Chun, and Xie Fengbao. The previous versions of this document and the documents it replaces are as follows. ---First issued in.1993 as YY 0177.2-1993, first revised in.2005; ---This is the second revision.

Introduction

YY 0117 "Surgical Implant Bone and Joint Prosthesis Forgings and Castings" consists of 3 parts. --- Part 1.Ti6Al4V titanium alloy forgings; --- Part 2.ZTi6Al4V titanium alloy castings; --- Part 3.Cobalt-chromium-molybdenum alloy castings. Due to the different materials used to manufacture forgings and castings of bone and joint prostheses, the corresponding performance indicators and test methods are different. The series of standards are divided into three parts, which respectively regulate forgings and castings of bone and joint prostheses made of different materials. This revision is a summary of the original standards. and improvement, aiming to standardize the manufacturing and quality control of forgings and castings of bone and joint prostheses. Surgical implants, bone and joint prostheses, forgings and castings Part 2.ZTi6Al4V titanium alloy castings

1 Scope

This document specifies the requirements, test methods, inspection and quality control of surgical implant bone and joint prosthesis castings made of ZTi6Al4V titanium alloy material. Regulations, quality certification, labeling, packaging, transportation and storage. This document applies to the production and acceptance of ZTi6Al4V titanium alloy castings for bone and joint prostheses.

2 Normative references

The contents of the following documents constitute essential clauses of this document through normative references in this document. For referenced documents without a date, only the version corresponding to that date applies to this document; for referenced documents without a date, the latest version (including all amendments) applies to This document. GB/T 228.1 Tensile test of metallic materials Part 1.Room temperature test method GB/T 4698 (all parts) Chemical analysis methods for titanium sponge, titanium and titanium alloys GB/T 10610 Geometric Product Specification (GPS) Rules and methods for evaluating surface structure by surface structure profile method GB/T 23603 Detection method for surface contamination layer of titanium and titanium alloys HB6103 Casting Dimension Tolerance and Machining Allowance HB6573 Standard reference radiographs for investment steel castings HB20160 X-ray photography inspection YY/T 0343 Liquid Penetrant Testing of Surgical Metal Implants YY/T 1565-2017 Non-destructive testing of surgical implants - Radiographic testing of cast metal surgical implants

3 Terms and definitions

There are no terms or definitions that require definition in this document.

4 Requirements

4.1 Raw materials 4.1.1 The raw materials for manufacturing bone and joint prosthesis castings should be ingots or forged bars. The ingots should be subjected to two or more vacuum or inert The forged rod is a rod obtained by forging the above-mentioned ingot and removing the oxide scale under gas protection. 4.1.2 The castings and test specimens may be cast from the same master alloy or from the same smelting furnace batch of a master alloy. 4.2 Chemical composition Carry out the test according to the method described in 5.1.The chemical composition of the casting shall conform to the provisions of Table 1. Other elements generally include. Sn, Mo, Cr, Mn, Zr, Ni, Cu, Si, Y (the alloy elements contained in this grade should be removed). The following items may not be tested. When the purchaser deems it necessary, random inspection may be carried out. The results of random inspection shall comply with the provisions of Table 1.
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