GB/T 16886.5-2017: Biological evaluation of medical devices -- Part 5: Tests for in vitro cytotoxicity

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Scope

This Part of GB/T 16886 describes test methods to assess the in vitro
cytotoxicity of medical devices.
This Part specifies the incubation of cultured cells in contact with a device
and/or extracts of a device either directly or through diffusion.

Basic Data

Standard ID	GB/T 16886.5-2017 (GB/T16886.5-2017)
Description (Translated English)	Biological evaluation of medical devices -- Part 5: Tests for in vitro cytotoxicity
Sector / Industry	National Standard (Recommended)
Classification of Chinese Standard	C30
Classification of International Standard	11.100.20
Word Count Estimation	34,387
Date of Issue	2017-12-29
Date of Implementation	2018-07-01
Issuing agency(ies)	General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China, Standardization Administration of the People's Republic of China