GB/T 16886.12-2017Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (English PDF)
医疗器械生物学评价 第12部分：样品制备与参照材料
GB/T 16886.12 | Evolution and historical versions
| Std ID | Title | Status |
|---|---|---|
| GB/T 16886.12-2023 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | Valid |
| GB/T 16886.12-2017 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | Obsolete |
GB/T 16886.12-2017 is obsolete. It has been replaced by GB/T 16886.12-2023. 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 29, 2017
Implementation date
July 1, 2018
Scope
GB/T 16886.12-2017 is the English-translated version of 医疗器械生物学评价 第12部分：样品制备与参照材料.
GB/T 16886.12-2017 is the Chinese national standard "Biological evaluation of medical devices - Part 12: Sample preparation and reference materials".
It was issued on December 29, 2017 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 July 1, 2018. It is obsolete: it has been replaced by GB/T 16886.12-2023.
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Document preview — GB/T 16886.12-2017
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: 2017-12-29.
Date of implementation: 2018-07-01.
Status: obsolete, replaced by GB/T 16886.12-2023.
......
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
- YY/T 0942-2026Ophthalmic optics. Injection system of intraocular lenses
- YY/T 1431-2026Implants for surgery. Medical-grade ultra-high molecular weight polyethylene yarns
- YY/T 1670.2-2025Neurotoxicity evaluation of medical devices - Part 2: Tests for neuro-cytotoxicity
- YY 0603-2024Cardiopulmonary bypass systems - Hard-shell cardiotomy/venous reservoirs (with or without filter) and soft venous reservoir bags
- YY/T 1535-2024Medical devices for human assisted reproductive technology - Human sperm viability assay (HSVA)
- GB 19083-2023Protective face masks for medical use
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Related Standards
GB/T 16886.13-2017 — Biological evaluation of medical devices-Part 13:Identification and quantification of degradation products from polymeric medical devices
GB/T 16886.11-1997 — Biological evaluation of medical devices--Part 11: Tests for systemic toxicity
GB/T 16886.13-2001 — Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices
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GB/T 16886.12-2017
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