GB/T 16886.6-2015Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (English PDF)
医疗器械生物学评价 第6部分：植入后局部反应试验
GB/T 16886.6 | Evolution and historical versions
| Std ID | Title | Status |
|---|---|---|
| GB/T 16886.6-2022 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation | Valid |
| GB/T 16886.6-2015 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation | Obsolete |
GB/T 16886.6-2015 is obsolete. It has been replaced by GB/T 16886.6-2022. This page sells the obsolete edition, for projects and contracts that still cite it.
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Issued by
General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China; Standardization Administration of China
Level / Type
National · Recommended
Issue date
December 10, 2015
Implementation date
April 1, 2017
Scope
GB/T 16886.6-2015 is the English-translated version of 医疗器械生物学评价 第6部分：植入后局部反应试验.
GB/T 16886.6-2015 is the Chinese national standard "Biological evaluation of medical devices - Part 6: Tests for local effects after implantation".
It was issued on December 10, 2015 by the General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China and the Standardization Administration of China, and took effect on April 1, 2017. It is obsolete: it has been replaced by GB/T 16886.6-2022.
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Document preview — GB/T 16886.6-2015
National Standard of the People's Republic of China
Issued by: General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China; Standardization Administration of China
Contents
- Document data
1 Document data
Sector: National standard (Recommended).
Issuing body: General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China; Standardization Administration of China.
Date of issue: 2015-12-10.
Date of implementation: 2017-04-01.
Status: obsolete, replaced by GB/T 16886.6-2022.
......
This preview omits tables, figures, formulas and parts of the technical clauses. The complete document — all pages — is available in the English PDF.
Referenced standards
Cited by
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- GB/T 44875-2024Fallopian rings - Requirements and test methods
- YY 0861-2024Ophthalmic optics - Ophthalmic viscosurgical devices
- YY/T 0127.19-2023Biological evaluation of medical devices used in dentistry - Part 19: Subacute and subchronic systemic toxicity test: implantation route
- YY/T 0606.15-2023Tissue engineered medical products - Standard practice for evaluation of immune response to matrices and scaffolds: lymphocyte proliferation test
- YY/T 1899-2023Preparation and evaluation methods of histopathological samples after implantation of absorbable medical devices
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Related Standards
GB/T 16886.7-2015 — Biological evaluation of medical devices—Part 7: Ethylene oxide sterilization residuals
GB/T 16886.5-2003 — Biological evaluation of medical devices - Part 5: Test for in vitro cytotoxicity
GB/T 16886.7-2001 — Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals
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GB/T 16886.6-2015
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