SNo |
IS Number |
Title |
Technical Committee |
1 |
IS/ISO 5356 : Part 1 : 2015 |
Anaesthetic and respiratory equipment - Conical connectors: Part 1 cones and sockets (First Revision) |
MHD 11 |
2 |
IS 17932 : Part 1 : 2023 |
Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process (ISO 10993-1 : 2018, MOD) |
MHD 19 |
3 |
IS/ISO 17664 : 2017 |
Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices |
MHD 12 |
4 |
IS/ISO 17664 : 2017 |
Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices |
MHD 12 |
5 |
IS/ISO 14937 : 2009 |
Sterilization of health care products General requirements for characterization of a sterilizing agent and the development validation and routine control of a sterilization process for medical devices |
MHD 12 |
6 |
IS/ISO 14971 : 2019 |
Medical devices - Application of risk management to medical devices First Revision |
MHD 14 |
7 |
IS 9000 : Part 7 : Sec 3 : 2019 |
Environmental testing: Part 7 tests :: Sec 3 test Ec: rough handling shocks, primarily for equipment - Types specimens (First Revision) |
LITD 1 |
8 |
IS 17922 : Part 1 : 2023 |
Medical Devices Part 1: Application of Usability Engineering |
MHD 14 |
9 |
IS/ISO 5356 : Part 1 : 2015 |
Anaesthetic and respiratory equipment - Conical connectors: Part 1 cones and sockets (First Revision) |
MHD 11 |
10 |
IS 17932 : Part 1 : 2023 |
Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process (ISO 10993-1 : 2018, MOD) |
MHD 19 |
11 |
IS/ISO 17664 : 2017 |
Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices |
MHD 12 |
12 |
IS/ISO 17664 : 2017 |
Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices |
MHD 12 |
13 |
IS/ISO 14937 : 2009 |
Sterilization of health care products General requirements for characterization of a sterilizing agent and the development validation and routine control of a sterilization process for medical devices |
MHD 12 |
14 |
IS/ISO 14971 : 2019 |
Medical devices - Application of risk management to medical devices First Revision |
MHD 14 |
15 |
IS 9000 : Part 7 : Sec 3 : 2019 |
Environmental testing: Part 7 tests :: Sec 3 test Ec: rough handling shocks, primarily for equipment - Types specimens (First Revision) |
LITD 1 |
16 |
IS 17922 : Part 1 : 2023 |
Medical Devices Part 1: Application of Usability Engineering |
MHD 14 |