| SNo |
IS Number |
Title |
Technical Committee |
|
1 |
IS 391 : 2020 |
Textile fabrics – Determination of resistance to water penetration – Hydrostatic pressure test (second revision) |
TXD 5 |
|
2 |
IS 1966 : Part 1 : 2022 |
Textiles - Bursting properties of fabrics Part 1: Hydraulic method for determination of bursting strength and bursting distension (third revision) |
TXD 1 |
|
3 |
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 |
|
4 |
IS 4905 : 2015 |
Random sampling and randomization procedures (First Revision) |
MSD 3 |
|
5 |
IS 15891 : Part 3 : 2024 |
Nonwovens — Methods of Test Part 3 Determination of Tensile Strength and Elongation at Break Using the Strip Method (First Revision) |
TXD 33 |
|
6 |
IS 15891 : Part 10 : 2017 |
Textiles - Test Methods for Nonwovens Part 10 Lint and Other Particle Generation in the Dry State |
TXD 33 |
|
7 |
IS 16390 : 2015 |
Agro textiles - Nylon knitted seamless gloves for tobacco harvesters - Specification |
TXD 35 |
|
8 |
IS 16545 : 2016 |
Clothing for protection against contact with blood and body fluids – Determination of resistance of protective clothing materials to penetration by blood-borne pathogens – Test method using Phi-X174 bacteriophage |
TXD 36 |
|
9 |
IS 16546 : 2016 |
Clothing for protection against contact with blood and body fluids - Determination of the resistance of protective clothing materials to penetration by blood and body fluids - Test method using synthetic blood |
TXD 36 |
|
10 |
IS 16548 : 2016 |
Clothing for protection against infectious agents - Test method for resistance to dry microbial penetration |
TXD 36 |
|
11 |
IS 16549 : 2020 |
Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment – Test method to determine the resistance to wet bacterial penetration (first revision) |
TXD 36 |
|
12 |
IS 17375 : 2020 |
Textiles – Determination of resistance to water penetration – Impact penetration test |
TXD 5 |
|
13 |
IS 17932 : Part 6 : 2023 |
Biological Evaluation of Medical Devices Part 6 Tests for skin sensitization (ISO 10993-10 : 2021, MOD) |
MHD 19 |
|
14 |
IS 17932 : Part 7 : 2024 |
Biological Evaluation of Medical Devices Part 7 Tests for irritation ISO 10993-23:2021 MOD |
MHD 19 |
|
15 |
IS 18637 : Part 1 : 2024 |
Cleanrooms and associated controlled environments Part 1: Classification of air cleanliness by particle concentration |
CHD 35 |
|
16 |
IS 18469 : Part 7 : 2023 |
Sterilization of health care products Biological indicators Part 7: Guidance for the selection use and interpretation of results |
MHD 12 |
|
17 |
IS/ISO 10993 : Part 5 : 2009 |
Biological evaluation of medical devices Part 5 Tests for in vitro cytotoxicity |
MHD 19 |
|
18 |
IS/ISO 10993 : Part 7 : 2018 |
Biological evaluation of medical devices Part 7 Ethylene oxide sterilization residuals |
MHD 19 |
|
19 |
IS/ISO 10993 : Part 12 : 2021 |
Biological Evaluation of Medical Devices Part 12 Sample Preparation and Reference Materials |
MHD 19 |
|
20 |
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 |
|
21 |
IS/ISO 11137 : Part 2 : 2013 |
Sterilization of health care products - Radiation: Part 2 establishing the sterilization dose |
MHD 12 |
|
22 |
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 |
|
23 |
IS/ISO 11607 : Part 1 : 2019 |
Packaging for terminally sterilized medical devices — Part 1: Requirements for materials sterile barrier systems and packaging systems First Revision |
MHD 12 |
|
24 |
IS/ISO 11607 : Part 2 : 2019 |
Packing for Terminally Sterilized Medical Devices Part 2 Validation Requirements for Forming Sealing and Assembly Processes (First Revision) |
MHD 12 |
|
25 |
IS/ISO 11737 : Part 1 : 2018 |
Sterilization of health care products Microbiological methods Part 1: Determination of a population of microorganisms on products |
MHD 12 |
