GB 11236-2006 Replaced National standards force_standard

GB 11236-2006 TCu intra-uterine devices

GB 11236-2006 TCu intra-uterine devices

Publish Date: 2006-09-14 Implement Date: 2007-05-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: GB 11236-2006
Standard Type: National standards
Standard Status: Replaced
is_force_gb: yes
CCS Name: Other specialized equipment
ICS Name: Medical equipment
Publish Date: 2006-09-14
Implement Date: 2007-05-01
Pages: 11 pages

Scope

This standard specifies the product characteristics, basic dimensions, materials, requirements, test methods, inspection rules, marking, packaging, storage, and sterilization validity period of the copper T-type TCu intrauterine contraceptive device with an accompanying placement device. This standard applies to the copper T-type TCu intrauterine contraceptive device (hereinafter referred to as the contraceptive device). This contraceptive device is placed in a woman's uterine cavity for contraception purposes.

Development Information

Word Count: 19 Thousand words Pages: 11 pages

Replace the following standards

Superseded by the following standards

Referenced Standards

GB/T 14233.1-1998 Infusion,transfusion,injection equipment for medical use—Part 1:Chemical analysis methods GB/T 16886.1-2001 Biological evaluation of medical devices—Part 1:Evaluation and testing JJG 455-2000 Working Dynamometers 中华人民共和国药典(2000年版) GB/T 191-2000 Packaging—Pictorial marking for handling of goods GB/T 191-2008 Packaging—Pictorial marking for handling of goods 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 2828.1-2012 Sampling procedures for inspection by attributes—Part 1:Sampling schemes indexed by acceptance quality limit(AQL) for lot-by-lot inspection GB 9969.1-1998 General principles for preparation of instructions for use of industrial products GB/T 13293.1-1991 Higher purity copper cathode—Determination of selenium and tellurum contents—Catalytic oscillopolarographic method GB/T 13293.2-1991 Higher purity copper cathode—Determination of bismuth content—Hydride generation-atomic fluorescence spectrometric method GB/T 13293.3-1991 Higher purity copper cathode—Determination of chromium, manganese and cadmium contents—Zeeman effect electrothermal atomic absorption spectrometric method GB/T 13293.4-1991 Higher purity copper cathode—Determination of antimony content-2-[(-5-bromo-2-pyridyl)azo]-5-diethylaminophenol spectrophotometric method GB/T 13293.5-1991 Higher purity copper cathode—Determination of arsenic content—Heteropoly arsenomolybdic acid-crystal violet spectrophotometric method GB/T 13293.6-1991 Higher purity copper cathode—Determination of phosphorus content—Heteropoly phosphato-vanadato-molybdicacid-crystal violet spectrophotometric method GB/T 13293.7-1991 Higher purity copper cathode—Determination of iron, cobalt and lead contents—Zeeman effect electrothermal atomic absorption spectrometric method GB/T 13293.8-1991 Higher purity copper cathode—Determination of nickel content—Zeeman effect electrothermal atomic absorption spectrometric method GB/T 13293.9-1991 Higher purity copper cathode—Determination of tin content—Zeeman effect electrothermal atomic absorption spectrometric method GB/T 13293.10-1991 Higher purity copper cathode—Determination of zinc content—Flame atomic absorption spectrometric method GB/T 13293.11-1991 Higher purity copper cathode—Determination of silicon content—Molybdenum blue spectrophotometric method GB/T 13293.12-1991 Higher purity copper cathode—Determination of silver content—Separation and preconcentration with sulfhydryl cotton-flame atomic absorption spectrometric method GB/T 13293.13-1991 Higher purity copper cathode—Determination of sulphur content—Combustion-potassium iodate titrimetric method GB/T 16886.5-2003 Biological evaluation of medical devices—Part 5:Test for in vitro cytotoxicity GB/T 16886.5-2017 Biological evaluation of medical devices—Part 5:Tests for in vitro cytotoxicity GB/T 16886.6-1997 Biological evaluation of medical devices—Part 6:Tests for local effects after implantation GB/T 16886.6-2015 Biological evaluation of medical devices—Part 6:Tests for local effects after implantation GB/T 16886.6-2022 Biological evaluation of medical devices—Part 6:Tests for local effects after implantation GB/T 16886.10-2000 Biological evaluation of medical devices—Part 10:Tests for irritation and sensitization GB/T 16886.10-2005 Biological evaluation of medical devices—Part 10:Tests for irritation and delayed-type hypersensitivity GB/T 16886.10-2017 Biological evaluation of medical devices—Part 10:Tests for irritation and skin sensitization GB/T 16886.10-2024 Biological evaluation of medical devices—Part 10:Tests for skin sensitization GB/T 16886.11-1997 Biological evaluation of medical devices—Part 11:Tests for systemic toxicity GB/T 16886.11-2011 Biological evaluation of medical devices—Part 11:Tests for systemic toxicity GB/T 16886.11-2021 Biological evaluation of medical devices—Part 11:Tests for systemic toxicity GB 18279-2000 Medical devices—Validation and routine control of ethylene oxide sterilization GB 18279-2023 Sterilization of health-care products—Ethylene oxide—Requirements for the development,validation and routine control of a sterilization process for medical devices GB 18279.1-2015 Sterilization of health care products—Ethylene oxide—Part 1:Requirements for development,validation and routine control of a sterilization process for medical devices GB/T 18279.2-2015 Sterilization of health care products—Part 2:Guidance on the application of GB 18279.1 GB/T 191-2025 Graphical symbols marking for handling and storage of packages

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