General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China
Latest
GB 24787-2009
Scope
This standard specifies the performance, safety and technical requirements for disposable non-sterile rubber surgical gloves. This standard applies to packaged non-sterile rubber surgical gloves used in surgical operations to prevent cross-infection between patients and users. However, the storage, safety, proper use, sterilization and subsequent handling of gloves do not apply to this standard.
GB 24787-2009 Referenced Document
GB/T 1.1 Directives for standardization—Part 1: Rules for the structure and drafting of standardizing documents*, 2020-03-31 Update
GB/T 1.2 Directives for standardization—Part 2:Drafting rules of standardizing documents based on ISO/IEC standardizing documents*, 2020-11-19 Update
GB/T 1.22 Directives for work of standardization Unit2:Methodology for the development of standards Part22:Rule of "reference to standards"
GB/T 1.4 Standardization Work Guidelines Chemical Analysis Method Standard Compilation Provisions
GB/T 1.6 Regulations on Compilation of Terminology Standards in Standardization Work Guidelines
GB/T 16886.1-2001 Biological evaluation of medical devices--Part 1: Evaluation and testing
GB/T 16886.10-2005 Biological evaluation of medical devices.Part 10:Tests for irritation and delayed-type hypersensitivity
GB/T 16886.11-1997 Biological evaluation of medical devices--Part 11: Tests for systemic toxicity
GB/T 16886.12-2000 Biological evaluation of medical devices--Part 12: Sample preparation and reference materials
GB/T 16886.13-2001 Biological evaluation of medical devices--Part 13:Identification and quantification of degradation products from polymeric medical devices
GB/T 16886.14-2003 Biological evaluation of medical devices--Part 14: Identification and quantification of degradation products from ceramics
GB/T 16886.15-2003 Biological eveluation of medical devices--Part 15: Identification and quantification of degradation products from metals and alloys
GB/T 16886.16-2003 Biological evaluation of medical devices--Part 16: Toxicokinetic study design for degradation products and leachables
GB/T 16886.17-2005 Biological evaluation of medical devices.Part 17:Establishment of allowable limits for leachable substances
GB/T 16886.2-2000 Biological evaluation of medical devices--Part 2: Animal welfare requirements
GB/T 2828.1-2003 Sampling procedures for inspection by attributes--Part 1: Sampling schemes indexed by acceptance quality limit(AQL) for lot-by-lot inspection
GB/T 2941-2006 Rubber. General procedures for preparing and conditioning test pieces for physical test methods
GB/T 3512-2001 Rubber,vulcanized or thermoplastic--Accelerated ageing and heat resistance tests-Air-oven method
GB/T 528-2009 Rubber,vulcanized or thermoplastic.Determination of tensile stress-strain properties