SNo |
IS Number |
Title |
Technical Committee |
1 |
IS 2500 : Part 1 : 2000 |
Sampling procedures for inspection by attributes: Part 1 sampling schemes indexed by acceptance quality limit (AQL) for lot - By - Lot inspection (Third Revision) |
MSD 3 |
2 |
IS 3400 : Part 1 : 2021 |
Methods of Test for Vulcanized Rubber Part 1 Tensile Stress-Strain Properties |
PCD 29 |
3 |
IS 3400 : Part 4 : 2012 |
Methods of test for vulcanized rubber: Part 4 accelerated ageing and heat resistance (Third Revision) |
PCD 29 |
4 |
IS/ISO 10993 : Part 3 : 2014 |
Biological evaluation of medical devices Part 3 Tests for Genotoxicity, Carcinogenicity and Reproductive toxicity (First Revision) |
MHD 19 |
5 |
IS/ISO 10993 : Part 4 : 2017 |
Biological evaluation of medical devices Part 4 Selection of tests for interactions with blood |
MHD 19 |
6 |
IS/ISO 10993 : Part 5 : 2009 |
Biological evaluation of medical devices Part 5 Tests for in vitro cytotoxicity |
MHD 19 |
7 |
IS/ISO 10993 : Part 6 : 2016 |
Biological evaluation of medical devices Part 6 Tests for local effects after implantation |
MHD 19 |
8 |
IS/ISO 10993 : Part 7 : 2018 |
Biological evaluation of medical devices Part 7 Ethylene oxide sterilization residuals |
MHD 19 |
9 |
IS/ISO 10993 : Part 9 : 2009 |
Biological evaluation of medical devices Part 9 Framework for identification and quantification of potential degradation products |
MHD 19 |
10 |
IS/ISO 10993 : Part 10 : 2010 |
Biological evaluation of medical devices Part 10 Tests for irritation and skin sensitization |
MHD 19 |
11 |
IS/ISO 10993 : Part 11 : 2017 |
Biological evaluation of medical devices Part 11 Tests for systemic toxicity |
MHD 19 |
12 |
IS/ISO 10993 : Part 15 : 2000 |
Biological evaluation of medical devices: Part 15 identification and quantification of degradation products from metals and alloys |
MHD 19 |
13 |
IS/ISO 10993 : Part 16 : 2017 |
Biological Evaluation of Medical Devices Part 16 Toxicokinetic Study Design for Degradation Products and Leachables |
MHD 19 |
14 |
IS/ISO 10993 : Part 17 : 2002 |
Biological Evaluation of Medical Devices Part 17 Establishment of Allowable Limits for Leachable Substances |
MHD 19 |
15 |
IS/IEC/TS 10993 : Part 19 : 2006 |
Biological Evaluation of Medical Devices Part 19 Physico-Chemical, Morphological and Topographical Characterization of Materials |
MHD 19 |
16 |
IS/ISO/TR 10993 : Part 22 : 2017 |
Biological Evaluation of Medical Devices Part 22 Guidance on Nanomaterials |
MHD 19 |
17 |
IS 13867 : 1993 |
Rubber - Standard temperatures, humidities and times for the conditioning and time interval between vulcanization and testing of test pieces |
PCD 29 |
18 |
IS 11159 : Part 3 : 1989 |
Classification of lubricants, industrial oils and related products: Part 3 family f (Spindle Bearings, Bearings And Associated Clutches) |
PCD 25 |
19 |
IS 11162 : Part 1 : 1985 |
Dimensions of non - Insulated terminal tags for electronic equipment: Part 1 type 1 |
LITD 3 |
20 |
IS 3758 : 2018 |
Hooks, aural - Specification (First Revision) |
MHD 4 |
21 |
IS 9298 : Part 2 : 1980 |
Specification for television pattern generators: Part 2 methods of measurements |
LITD 8 |
22 |
IS 9835 : 1981 |
Specification for series capacitors for power systems |
ETD 29 |
23 |
IS 9835 : Part 1 : 2001 |
Series Capacitors for Power Systems - Part 1 : General Performance, Testing and Rating - Safety Requirements - Guide for Installation |
ETD 29 |