IS 17423 : 2021 — Medical Textiles — Bio-Protective Coveralls — Specification (First Revision)

What is IS 17423 : 2021?

IS 17423 : 2021 is an Indian Standard published by the Bureau of Indian Standards (BIS) under the title Medical Textiles — Bio-Protective Coveralls — Specification (First Revision). It falls under the <strong>Textile, Textile Products and Machinery</strong> group and is administered by the Ministry of Textiles. Certification under this standard is voluntary.

How to get certified for IS 17423 : 2021

1. 1
   Apply online — Submit the BIS portal application with product details, factory information, and test reports.
2. 2
   Lab testing — Submit product samples to a BIS-recognised testing laboratory for evaluation against the standard.
3. 3
   Factory inspection — A BIS officer visits your manufacturing facility to verify quality control systems.
4. 4
   Licence grant — On approval, BIS issues the licence. You may then affix the ISI Mark on compliant products.

Amendments to IS 17423 : 2021

Related Indian Standards

• IS 15891Textiles - Test Methods for Nonwovens Part 15 Determination of Air Rermeability
• IS 15891Textiles - Test Methods for Nonwovens Part 15 Determination of Air Rermeability
• IS 16390Agro textiles - Nylon knitted seamless gloves for tobacco harvesters - Specification
• IS 16545Clothing 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
• IS 16546Clothing 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
• IS 1966Textiles - Bursting properties of fabrics Part 2: Pneumatic method for determination of bursting strength and bursting distension (third revision)
• IS 1969Textiles — Tensile Properties of Fabrics Part 1 Determination of Maximum force and Elongation at Maximum Force Using the Strip Method ( Fourth Revision )
• IS 4905Random sampling and randomization procedures (First Revision)
• IS/ISO 10993 : Part 10 : 2010Biological evaluation of medical devices Part 10 Tests for irritation and skin sensitization
• IS/ISO 10993 : Part 5 : 2009Biological evaluation of medical devices Part 5 Tests for in vitro cytotoxicity
• IS/ISO 10993 : Part 7 : 2018Biological evaluation of medical devices Part 7 Ethylene oxide sterilization residuals
• IS/ISO 11135 : 2014Sterilization of health - Care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices
• IS/ISO 11137 : Part 1 : 2006Sterilization of health care products - Radiation: Part 1 requirements for development, validation and routine control of a sterilization process for medical devices
• IS/ISO 11137 : Part 2 : 2013Sterilization of health care products - Radiation: Part 2 establishing the sterilization dose
• IS/ISO 11607 : Part 1 : 2019Packaging for terminally sterilized medical devices — Part 1: Requirements for materials sterile barrier systems and packaging systems First Revision
• IS/ISO 11607 : Part 2 : 2019Packing for Terminally Sterilized Medical Devices Part 2 Validation Requirements for Forming Sealing and Assembly Processes (First Revision)
• IS/ISO 13935 : Part 1 : 2014Textiles - Seam tensile properties of fabrics and made-up textile articles Part 1 Determination of maximum force to seam rupture using the strip method (first revision)
• ISO 11138 (Part 7):2019ISO 11138 (Part 7):2019
• ISO 11737 (Part 1):2018ISO 11737 (Part 1):2018
• ISO 14644 (Part 1):2015ISO 14644 (Part 1):2015
• ISO 14698 (Part 1):2003ISO 14698 (Part 1):2003
• ISO 17665 (Part 1):2006ISO 17665 (Part 1):2006