Role of Establishment of Allowable Limits for Leachable Substances in Safety Evaluation of Medical Devices.
10.12455/j.issn.1671-7104.240016
- Author:
Fangming XU
1
Author Information
1. Zhejiang Institute of Medical Device Testing, Hangzhou,
- Publication Type:Journal Article
- Keywords:
allowable limits;
leachable substances;
medical device;
risk management;
safety evaluation
- MeSH:
Equipment and Supplies/standards*;
Equipment Safety
- From:
Chinese Journal of Medical Instrumentation
2025;49(1):103-110
- CountryChina
- Language:Chinese
-
Abstract:
The objective of inspection, testing and supervision of medical devices is to ensure the effectiveness and safety of medical devices in use. Leachables are substances that are leached from medical devices or materials during their clinical use. Leachables are important factors for the safety risks of medical devices. The analysis, detection, and safety evaluation of leachables are important parts of the safety evaluation of medical devices. The allowable limits for leachable substances which are established on the toxicological research provide a scientific basis for the judgment of qualitative and quantitative analysis results. Obtaining more detailed, rigorous and sufficient toxicological research data is of great significance to set highly enforceable product technical indicators. For the establishment of allowable limits for leachable substances, its role in the safety evaluation of medical devices is summarized, and the relevant standards and their implementation status in the testing of medical devices are introduced.
