GB/T 16886.11-1997
Replaced
T/CIET 1032-2025
Active
Group standards
T/CIET 1032-2025 The reliability evaluation requirements for silicone hydrogel contact lenses
T/CIET 1032-2025 The reliability evaluation requirements for silicone hydrogel contact lenses
Price:
$ 20.00
Basic Information
Standard Code:
T/CIET 1032-2025
Standard Type:
Group standards
Standard Status:
Active
is_force_gb:
no
CCS Name:
-
ICS Name:
Integrated medical equipment
Publish Date:
2025-02-19
Implement Date:
2025-02-19
Scope
Scope: This document specifies the basic requirements, evaluation indicators and methods, reliability determination principles, evaluation indicators and methods, and evaluation results and reports for the reliability evaluation of silicone hydrogel contact lenses. This document is applicable to the evaluation of silicone hydrogel contact lenses; Main technical content: This document specifies the basic requirements, evaluation indicators and methods, reliability determination principles, evaluation indicators and methods, and evaluation results and reports for the reliability evaluation of silicone hydrogel contact lenses. This document is applicable to the evaluation of silicone hydrogel contact lenses.
Development Information
Related Standards
GB/T 16886.3-1997
Replaced
GB/T 16886.3-1997 Biological evaluation of medical devices—Part 3:Tests for genotoxicity, carcinogenicity and reproductive toxicity
GB/T 16886.6-1997
Replaced
GB/T 16886.6-1997 Biological evaluation of medical devices—Part 6:Tests for local effects after implantation
GB/T 16886.1-2001
Replaced
GB/T 16886.1-2001 Biological evaluation of medical devices—Part 1:Evaluation and testing
GB/T 16886.13-2001
Replaced
GB/T 16886.13-2001 Biological evaluation of medical devices—Part 13:Identification and quantification of degradation products from polymeric medical devices
GB/T 16886.7-2001
Replaced