UNLIMITED FREE
ACCESS TO THE WORLD'S BEST IDEAS

SUBMIT
Already a GlobalSpec user? Log in.

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

Customize Your GlobalSpec Experience

Select Your Free Newsletters

Industry Newsletters

Select Your Free Product Alerts

Finish!
Privacy Policy

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

ISO 20308

Traditional Chinese medicine - Gua Sha instruments

active, Most Current
Buy Now
Organization: ISO
Publication Date: 1 May 2017
Status: active
Page Count: 20
ICS Code (Other medical equipment): 11.040.99
scope:

This document specifies appearance, material, requirements of visual inspection, cleaning and disinfection, hardness, roughness, resistance to abrasion, exposure index of radionuclide activity, biocompatibility of Gua Sha instruments, as well as related information on package, transport and storage, labelling and instructions for use.

Electro-devices and other forms are outside the scope of this document

Document History

ISO 20308
May 1, 2017
Traditional Chinese medicine - Gua Sha instruments
This document specifies appearance, material, requirements of visual inspection, cleaning and disinfection, hardness, roughness, resistance to abrasion, exposure index of radionuclide activity,...

References

This document references:
ISO 10993-1 - Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
Published by ISO on August 1, 2018
This document specifies: — the general principles governing the biological evaluation of medical devices within a risk management process; — the general categorization of medical devices based on the...
This document references:
10993-10 - Biological evaluation of medical devices — Part 10: Tests for skin sensitization
Published by ISO on November 1, 2021
This document specifies the procedure for the assessment of medical devices and their constituent materials with regard to their potential to induce skin sensitization. This document includes: —...
This document references:
ISO 10993-18 - Biological evaluation of medical devices — Part 18: Chemical characterization of medical device materials within a risk management process
Published by ISO on January 1, 2020
This document specifies a framework for the identification, and if necessary, quantification of constituents of a medical device, allowing the identification of biological hazards and the estimation...
This document references:
ISO 17664 - Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices
Published by ISO on October 1, 2017
This document specifies requirements for the information to be provided by the medical device manufacturer for the processing of a medical device that requires cleaning followed by disinfection...
This document references:
ISO TS 10993-19 - Biological evaluation of medical devices — Part 19: Physico-chemical, morphological and topographical characterization of materials
Published by ISO on March 1, 2020
This document provides a compilation of parameters and test methods that can be useful for the identification and evaluation of the physical, i.e. physico‑chemical, morphological and topographical...
This document references:
ISO/IEC GUIDE 37 - Instructions for use of products by consumers
Published by ISO on December 1, 2012
This Guide establishes principles and gives recommendations on the design and formulation of instructions for use of products by consumers. This Guide is intended to be used by the following: -...
View Less
View All
Advertisement