SNo |
IS Number |
Title |
Technical Committee |
1 |
IS/ISO 105-E04 : 2008 |
Textiles ¬ Tests for colour fastness Part E04 Colour fastness to perspiration |
TXD 05 |
2 |
IS/ISO 105-C06 : 2010 |
Textiles – Tests for colour fastness Part C06 Colour fastness to domestic and commercial laundering (first revision) |
TXD 5 |
3 |
IS/ISO 105-X12 : 2016 |
Textiles – Tests for colour fastness Part X12 Colour fastness to rubbing (first revision) |
TXD 5 |
4 |
IS/ISO 105 : Part B02 : 2014 |
Textiles – Tests for colour fastness – Part B02 Colour fastness to artificial light: Xenon arc fading lamp test |
TXD 5 |
5 |
IS 1383 : 1977 |
Methods for determination of scouring loss in grey and finished cotton textile materials (first revision) |
TXD 5 |
6 |
IS 1390 : 2019 |
Textiles – Determination of pH of aqueous extract (second revision) |
TXD 5 |
7 |
IS 1966 : Part 1 : 2009 |
Textiles – Bursting properties of fabrics – Determination of bursting strength and bursting distension Part 1 Hydraulic method (second revision) |
TXD 1 |
8 |
IS 1969 : Part 1 : 2018 |
Textiles – Tensile properties of fabrics – Part 1 Determination of maximum force and elongation at maximum force using the strip method (fourth revision) |
TXD 1 |
9 |
IS 4905 : 2015 |
Random sampling and randomization procedures (First Revision) |
MSD 3 |
10 |
IS 10971 : PART 2 : 2011 |
Textiles – Determination of fabric propensity to surface fuzzing and to pilling Part 2 Modified Martindale method (first revision) |
TXD 1 |
11 |
IS/ISO 10993 : Part 5 : 2009 |
Biological evaluation of medical devices Part 5 Tests for in vitro cytotoxicity |
MHD 19 |
12 |
IS/ISO 10993 : Part 7 : 2018 |
Biological evaluation of medical devices Part 7 Ethylene oxide sterilization residuals |
MHD 19 |
13 |
IS/ISO 10993 : Part 10 : 2010 |
Biological evaluation of medical devices Part 10 Tests for irritation and skin sensitization |
MHD 19 |
14 |
IS/ISO 11135 : 2014 |
Sterilization of health - Care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices |
MHD 12 |
15 |
IS/ISO 11137 : Part 1 : 2006 |
Sterilization of health care products - Radiation: Part 1 requirements for development, validation and routine control of a sterilization process for medical devices |
MHD 12 |
16 |
IS 11137 : PART 2 : 2012 |
Analysis techniques for system reliABility: Part 2 procedure for failure mode and effects analysis (Fmea) (First Revision) |
LITD 2 |
17 |
IS/ISO 11607 : Part 1 : 2006 |
Packaging for terminally sterilized medical devices: Part 1 requirements for materials, sterile barrier systems and packaging systems |
MHD 12 |
18 |
IS/ISO 11607 : Part 2 : 2006 |
Packaging for terminally sterilized medical devices: Part 2 validation requirements for forming, sealing and assembly processes |
MHD 12 |
19 |
IS 14944 : 2020 |
Surgical Dressings - Methods of Test ( first revision ) |
TXD 36 |
20 |
IS 15370 : 2020 |
Textiles – Domestic washing and drying procedures for textiles testing (first revision) |
TXD 5 |
21 |
IS 15891 : Part 3 : 2011 |
Textiles - Test Methods for Nonwovens Part 3 Determination of Tensile Strength and Elongation |
TXD 33 |
22 |
IS 15891 : Part 10 : 2017 |
Textiles - Test Methods for Nonwovens Part 10 Lint and Other Particle Generation in the Dry State |
TXD 33 |
23 |
IS 15891 : Part 18 : 2017 |
Textiles - Test Methods for Nonwovens Part 18 Determination of Breaking Strength and Elongation of Nonwoven Materials Using the Grab Tensile Test |
TXD 33 |
24 |
IS 17376 : 2020 |
Textiles – Determination of physiological effects – Measurement of thermal and water-vapour resistance under steady-state conditions (Sweating guarded-hot plate test) |
TXD 5 |