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YY/T 1950-2024: Tissue engineering medical device - Silk fibroin
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Tissue engineering medical device - Silk fibroin
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YY/T 1950-2024
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Basic data | Standard ID | YY/T 1950-2024 (YY/T1950-2024) | | Description (Translated English) | Tissue engineering medical device - Silk fibroin | | Sector / Industry | Medical Device & Pharmaceutical Industry Standard (Recommended) | | Classification of Chinese Standard | C30 | | Classification of International Standard | 11.030.30 | | Word Count Estimation | 22,259 | | Date of Issue | 2024-09-29 | | Date of Implementation | 2025-10-15 | | Issuing agency(ies) | State Drug Administration | | Summary | This standard specifies the performance requirements of silk fibroin for tissue engineering medical device products, as well as the requirements for labeling, packaging, transportation and storage, and specifies the corresponding test methods. This standard is applicable to silk fibroin for the preparation of tissue engineering medical device products. | YY/T 1950-2024: Tissue engineering medical device - Silk fibroin---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 11.030.30
CCSC30
Pharmaceutical Industry Standards of the People's Republic of China
Tissue Engineering Medical Devices Silk Fibroin
Released on 2024-09-29
Implementation on October 15, 2025
The State Drug Administration issued
Table of Contents
Preface III
Introduction IV
1 Scope 1
2 Normative references 1
3 Terms and Definitions 1
4 Categories 2
5 Requirements for Animal Origin Materials 2
6 Performance requirements 2
7 Test methods 4
8 Stability 6
9 Packaging, transportation and storage 6
Appendix A (Informative) Research progress on basic structural characteristics and preparation methods of silk fibroin 7
Appendix B (Normative) Determination of Molecular Weight of Regenerated Silk Fibroin---Rheological Method 9
Reference 14
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 proposed by the State Food and Drug Administration.
This document is organized by the National Technical Committee for Standardization of Surgical Implants and Orthopedic Devices, Technical Committee for Engineering Medical Device Products
(SAC/TC110/SC3) is responsible for this matter.
This document was drafted by. Zhejiang University, China Food and Drug Administration, Fudan University, Zhejiang Xingyue Biotechnology Co., Ltd.
Co., Ltd., Fuxiang Sitai Medical Technology (Suzhou) Co., Ltd., and Jiangxi Sike Biotechnology Co., Ltd.
The main drafters of this document are. Ouyang Hongwei, Xu Liming, Shao Zhengzhong, Zhao Hongshi, Liu Yezhuo, Liu Keyin, Liu Zhenqi, Wang Yanyan, Chen Xin,
Yang Wenhua, Yang Tao, and Liu Li.
Introduction
The issuing authority of this document draws attention to the fact that claims of compliance with this document may involve the determination of molecular weight by rheological method in Appendix B.
The use of patents related to methods and data fitting calculations.
The issuing organization of this document takes no position on the authenticity, validity and scope of this patent.
The patent holder has promised to the issuing agency of this document that Appendix B has publicly provided the method operation instructions. The patent holder is willing to
The patent holder intends to share the application of this method with any user of the standard under reasonable and non-discriminatory terms and conditions.
The issuing agency of this document is on record. Relevant information can be obtained through the following contact information.
Patent holder name. Fudan University
Address. No. 220 Handan Road, Shanghai
Please note that in addition to the above patents, some of the contents of this document may still involve patents. The issuing agency of this document does not assume the responsibility for identifying patents
responsibility.
Tissue Engineering Medical Devices Silk Fibroin
1 Scope
This document specifies the performance requirements of silk fibroin used in tissue engineering medical device products, as well as the labeling, packaging, transportation and storage.
requirements and describes the corresponding test methods.
This document applies to silk fibroin for the preparation of tissue engineering medical device products.
Note 1.The silk fibroin referred to in this document is the product obtained by removing the sericin from the cocoon layer or raw silk of natural silkworms (i.e. natural silk fibroin fiber).
Products obtained by processes such as degumming, dissolution and regeneration (i.e. regenerated silk fibroin). It does not include silk fibroin obtained by genetic engineering or genetic modification.
protein.
Note 2.For silk fibroin used in other surgical implants or dressing products, refer to this document.
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 16886 (all parts) Biological evaluation of medical devices
GB/T 32016 Determination of amino acids in silk
FZ/T 40006 Test method for oil content of silk
SN/T 2843 Determination of rubber content in raw silk
YY/T 0771.1 Medical devices of animal origin Part 1.Application of risk management
YY/T 0771.2 Medical devices of animal origin Part 2.Control of sources, collection and disposal
YY/T 0771.3 Medical devices of animal origin Part 3.Removal and inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents
confirm
YY/T 1465 (all parts) Methods for evaluating the immunogenicity of medical devices
Pharmacopoeia of the People's Republic of China 2020 Edition
3 Terms and definitions
The following terms and definitions apply to this document.
3.1
Silk fibroin
Fibrous silk protein synthesized and secreted by the posterior silk gland of the silkworm.
Note. The core protein in mulberry silk fiber consists of a heavy chain (H chain protein) with a theoretical molecular mass of about 391 kDa, a light chain (L chain protein) of 25 kDa and a
kDa or 27kDa P25 (also called fiber hexamer), the amount ratio of H chain protein, L chain protein and P25 protein is 6.6.1.
The heavy chain and light chain are connected by a single disulfide bond. P25 is a glycoprotein containing asparagine (ASN) oligosaccharide chains. P25 is connected to the heavy chain and light chain by a disulfide bond.
They are bound by non-covalent bonds such as hydrophobic bonds.
3.2
Regenerated Silk Protein
Silk core fiber (fibroin fiber) dissolves the protein mixture after desalting.
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