T/CIET 932-2024 Active Group standards

T/CIET 932-2024 Soluble silk protein technical specification

Publish Date: 2024-12-25 Implement Date: 2024-12-25 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Price: $ 20.00

Out of stock

Basic Information

Standard Code: T/CIET 932-2024

Standard Type: Group standards

Standard Status: Active

is_force_gb: no

CCS Name: -

ICS Name: Integrated medical equipment

Publish Date: 2024-12-25

Implement Date: 2024-12-25

Scope

Scope: This document specifies the technical requirements and test items, test methods, inspection rules, marking, packaging, transportation, and storage for soluble silk fibroin. This document applies to the quality control of soluble silk fibroin solid materials, including soluble silk fibroin powder, soluble silk fibroin fiber, soluble silk fibroin beads, soluble silk fibroin porous materials, soluble silk fibroin membranes, and soluble silk fibroin aerogels, which are made from raw silk obtained directly from silkworm cocoons or silk cocoons and processed through crushing, dissolution, degradation, or purification. Main technical content: This document specifies the technical requirements and test items, test methods, inspection rules, marking, packaging, transportation, and storage for soluble silk fibroin. This document applies to the quality control of soluble silk fibroin solid materials, including soluble silk fibroin powder, soluble silk fibroin fiber, soluble silk fibroin beads, soluble silk fibroin porous materials, soluble silk fibroin membranes, and soluble silk fibroin aerogels, which are made from raw silk obtained directly from silkworm cocoons or silk cocoons and processed through crushing, dissolution, degradation, or purification.

Development Information

Related Standards

GB/T 16886.11-1997 Replaced

GB/T 16886.11-1997 Biological evaluation of medical devices—Part 11:Tests for systemic toxicity

Publish Date: 1997-06-26

GB/T 16886.3-1997 Replaced

GB/T 16886.3-1997 Biological evaluation of medical devices—Part 3:Tests for genotoxicity, carcinogenicity and reproductive toxicity

Publish Date: 1997-06-26

GB/T 16886.6-1997 Replaced

GB/T 16886.6-1997 Biological evaluation of medical devices—Part 6:Tests for local effects after implantation

Publish Date: 1997-06-26

GB/T 16886.1-2001 Replaced

GB/T 16886.1-2001 Biological evaluation of medical devices—Part 1:Evaluation and testing

Publish Date: 2001-09-24

GB/T 16886.13-2001 Replaced

GB/T 16886.13-2001 Biological evaluation of medical devices—Part 13:Identification and quantification of degradation products from polymeric medical devices

Publish Date: 2001-09-24

GB/T 16886.7-2001 Replaced

GB/T 16886.7-2001 Biological evaluation of medical devices—Part 7:Ethylene oxide sterilization residuals

Publish Date: 2001-09-24