GB 11234-2006 Replaced National standards force_standard

GB 11234-2006 Uterine cavity form intra-uterine devices

GB 11234-2006 Uterine cavity form 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 11234-2006
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 materials, types, basic dimensions, configurations, markings, requirements, test methods, inspection rules, labels, packaging, transportation, and storage of intrauterine devices (IUDs) with a cavity shape. This standard applies to intrauterine devices (hereinafter referred to as IUDs) with a cavity shape. This product is placed in a woman's uterine cavity for contraceptive purposes.

Development Information

Word Count: 16 Thousand words Pages: 11 pages

Replace the following standards

Superseded by the following standards

Referenced Standards

GB/T 191-2000 Packaging—Pictorial marking for handling of goods GB/T 4240-1993 Stainless steel wires GB/T 4340.1-1999 Metallic materials—Vickers hardness test—Part 1:Test method GB 9969.1-1998 General principles for preparation of instructions for use of industrial products GB/T 14233.1-1998 Infusion,transfusion,injection equipment for medical use—Part 1:Chemical analysis methods 中华人民共和国药典(2000年版) 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/T 16886.1-2001 Biological evaluation of medical devices—Part 1:Evaluation and testing GB/T 16886.1-2011 Biological evaluation of medical devices—Part 1:Evaluation and testing within a risk management process GB/T 16886.1-2022 Biological evaluation of medical devices—Part 1:Evaluation and testing within a risk management process 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 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 YY/T 0149-2006 Medical instruments of stainless steel—Test methods of corrosion resistance YY/T 0149-1993 Test method for corrosion resistance of stainless steel medical instruments

Related Standards

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