GB/T 35594-2017 Replaced National standards

GB/T 35594-2017 Medical packaging paper

GB/T 35594-2017 Medical packaging paper

Publish Date: 2017-12-29 Implement Date: 2018-07-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: GB/T 35594-2017
Standard Type: National standards
Standard Status: Replaced
is_force_gb: no
CCS Name: Paper
ICS Name: Paper and cardboard
Publish Date: 2017-12-29
Implement Date: 2018-07-01
Pages: 6 pages

Scope

This standard specifies the classification, requirements, test methods, inspection rules, marking, packaging, storage, and transportation of medical packaging paper. This standard applies to the production paper used for ethylene oxide sterilization and radiation sterilization of medical packaging.

Development Information

Word Count: 10 Thousand words Pages: 6 pages

Superseded by the following standards

Referenced Standards

GB/T 1545-2008 Paper,board and pulp—Determination of acidity or alkalinity GB/T 2678.2-2008 Paper, board and pulp—Determination of water soluble chlorides GB/T 458-2008 Paper and board—Determination of air permeance GB/T 450-2002 Paper and board—Sampling for testing GB/T 450-2008 Paper and board—Sampling for testing and identification of machine and cross direction,wire side and felt side GB/T 451.1-2002 Paper and board—Determination of size and deviation GB/T 451.2-2002 Paper and board—Determination of grammage GB/T 451.2-2023 Paper and board—Part 2:Determination of grammage GB/T 454-2002 Paper—Determination of bursting strength GB/T 454-2020 Paper—Determination of bursting strength GB/T 455-2002 Paper and board determination of tearing resistance GB/T 456-2002 Paper and board—Determination of smoothness (Bekk method) GB/T 462-2003 Paper and board—Determination of moisture content GB/T 462-2008 Paper,board and pulp—Determination of moisture content of analytical sample GB/T 462-2023 Paper, board and pulps—Determination of moisture content of analytical sample GB/T 465.1-2008 Paper and board—Determination of bursting strength after immersion in water GB/T 465.2-2008 Paper and board—Determination of tensile strength after immersion in water GB/T 1540-2002 Paper and board-Determination of water absorption-Cobb method GB/T 2678.6-1996 Paper, board and pulp—Determination of water soluble sulphates (Conductimetric titration method) GB/T 2678.6-2023 Paper,board and pulp—Determination of water-soluble sulfates 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 7974-2002 Paper, board and pulp-Measurement of brightness—Diff/Geometry GB/T 7974-2013 Paper,board and pulps—Measurement of diffuse blue reflectance factor—D65 brightness(Diff/ Geometry,Outdoor daylight conditions) GB/T 10342-2002 Paper—Package and mark GB/T 10739-2002 Paper, board and pulps—Standard atmosphere for conditioning and testing GB/T 10739-2023 Paper,board and pulps—Standard atmosphere for conditioning and testing GB/T 12914-1991 Paper and board—Determination of tensile properties—Constant rate of elongation method GB/T 12914-2008 Paper and board—Determination of tensile properties GB/T 12914-2018 Paper and board—Determination of tensile properties—Constant rate of elongation method(20 mm/min) GB/T 19633-2005 Packaging for terminally sterilized medical devices GB/T 19633.1-2015 Packaging for terminally sterilized medical devices—Part 1:Requirements for materials, sterile barrier systems and packaging systems GB/T 19633.1-2024 Packaging for terminally sterilized medical devices—Part 1:Requirements for materials,sterile barrier systems and packaging systems GB/T 19633.2-2015 Packaging for terminally sterilized medical devices—Part 2:Validation requirements for forming,sealing and assembly processes GB/T 19633.2-2024 Packaging for terminally sterilized medical devices—Part 2:Validation requirements for forming,sealing and assembly processes

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