Obtaining a BIS certificate for Anaesthetic, Resuscitation, And Allied Equipment (MHD-11) is essential. This certification ensures that the devices comply with stringent safety and quality standards, reinforce reliability, protect public health, and ensure adherence to regulatory guidelines.

This article explores the BIS Certification for anaesthetics, resuscitation, and allied equipment, highlighting its importance for manufacturers and the healthcare sector. We delve into how this certification supports industry standards, enhances product reliability, and improves patient care. Whether you are a manufacturer pursuing certification or a healthcare professional seeking to understand its impact, this comprehensive guide will address your queries and illustrate the benefits of BIS certification.

What Is BIS Certification?

The Bureau of Indian Standards (BIS) certification officially acknowledges that a product meets the prescribed safety, quality, and performance standards set by BIS. This certification involves comprehensive testing and evaluation, ensuring the product is safe and adheres to national regulatory requirements.

Importance Of Obtaining BIS Certificate For Anaesthetic, Resuscitation, And Allied Equipment?

Anaesthetic and resuscitation equipment play a vital role in life-saving medical procedures, where precision and reliability are paramount to patient safety. The various importance of BIS certification are:

  • Quality Assurance: BIS certification promises that anaesthetic, resuscitation, and allied equipment meet stringent quality and safety standards, critical for surgical and treatment efficacy.
  • Guarantee Safety Standards: It minimizes infection and complications by ensuring instruments are crafted from high-quality, safe materials.
  • Regulatory Compliance: Required by healthcare facilities and regulatory bodies, it ensures adherence to national standards and facilitates market entry.
  • Consumer Trust: BIS certification builds confidence in healthcare professionals and patients about the instrument’s reliability and performance.
  • Market Access: Recognized as a quality benchmark, it enhances opportunities in domestic and international markets.
  • Risk Mitigation: The certification process includes rigorous testing and evaluation, enabling early detection of potential issues to minimize risks during product use.
  • Competitive Edge: BIS certification distinguishes your products in a competitive market, enhancing their appeal and credibility over uncertified alternatives.

Also Read: BIS Certificate For Medical Laboratory Instruments

Who Needs BIS Certification For Anaesthetic, Resuscitation, And Allied Equipment?

The following entities are eligible to apply for BIS Certificate for anaesthetic, resuscitation, and allied equipment:

  1. Manufacturers: Producers intending to sell anaesthetic, resuscitation, and allied equipment in the Indian market.
  2. Importers: Individuals or entities seeking to import and distribute in India.
  3. Authorized Representatives: Designated individuals acting on behalf of manufacturers, importers, or foreign entities to obtain BIS certification.

Process To Obtain BIS Certificate For Anaesthetic, Resuscitation, And Allied Equipment

If you’re uncertain about the process of obtaining a BIS certificate for anaesthetic, resuscitation, and allied equipment, here’s a simplified guide to help:

  1. Identify Applicable Standards: Determine the relevant BIS standards and understand the safety and quality criteria outlined in the relevant Indian Standards.
  2. Organize Required Documents: Compile necessary documentation, including QMS details, technical data, manufacturing processes, and testing reports.
  3. Establish a QMS: Implement a Quality Management System that aligns with ISO 13485 to maintain consistent production quality.
  4. Submit Your Application: File your application with BIS, ensuring all documents are complete, and pay the required fee online or at the BIS office.
  5. Prepare for Factory Inspection: Allow BIS officials to audit your facility and processes for compliance with prescribed standards.
  6. Complete Product Testing: Ensure your products undergo testing at a BIS-approved lab to verify conformity with applicable standards.
  7. Issuance Of BIS Certificate: After successful testing and inspection, receive the BIS certificate, authorizing the use of the BIS mark on your products.

Also Read: BIS Certification For Medical Devices

Documents Required To Get BIS Certificate For Anaesthetic, Resuscitation, And Allied Equipment

Below is the essential documentation required to obtain a BIS certificate for anaesthetic, resuscitation, and allied equipment:

  • Completed Application Form
  • Quality Management System (QMS) Documentation
  • Technical Specifications
  • Manufacturing Process Details
  • Safety and Performance Test Reports
  • Product Labels and User Manuals
  • Certificate of Incorporation
  • Declaration of Conformity
  • Previous BIS Certifications
  • Fee Payment Proof

What Are The Indian Standards For Anaesthetic, Resuscitation, And Allied Equipment (MHD-11)?

Here we have listed down the Indian standards for BIS certificate for anaesthetic, resuscitation, and allied equipment (MHD 11), you can check them here:

SI. No.IS No.Title
1IS 11378: 2002/ISO 5358Anaesthetic machines for use with humans (First Revision)
(1 Revision)
2IS 12417: 1988Specification for suction apparatus, pedal-operated
3IS 13200: 2015/ISO 4135: 2001Anaesthetic and respiratory equipment – Vocabulary (First Revision)
(1 Revision)
4IS 17426: 2020ICU Ventilators for Use in COVID-19 — Specification
5IS 17587: 2021Specification for Pedal operated resuscitator
6IS 17625: Part 2: Sec 69 :2021/ISO 80601-2-69: 2020Medical Electrical Equipment Part 2 Particular Requirements for Basic Safety and Essential Performance Section 69 Oxygen Concentrator Equipment
7IS 3390: 1988Specification for sphygmomanometers, mercurial (Second Revision)
(2 Revision)
8IS 3391: 1965Specification for stethoscopes
9IS 3392: 1965Specification for anaesthetic airways
10IS 3393: 1965Specification for mouth props and airways (London Hospital Pattern)
11IS 4113: Part 1: 2003/ISO 7376: Part 1Laryngoscopic fittings: Part 1 conventional hook – On type handle – Blade fittings (Second Revision)
(2 Revision)
12IS 4113: Part 2: 2003/ISO 7376: Part 2Laryngoscopic fittings: Part 2 miniature electric lamps – Screw threads and sockets for conventional blades (Second Revision)
(2 Revision)
13IS 4154: 1967Specification for endotracheal connections
14IS 4533: 1995Suction apparatus – Specification (Second Revision)
(2 Revision)
15IS 5622: 1970Soda-Lime Canisters for Use with Gas Anaesthetic Apparatus ( Waters’ to-and-Fro)
16IS 5680: 1969Specification for rubber tubing for medical use
17IS 6190: 1971Specification for anaesthetic face masks
18IS 6194: 1971Specification for intermittent positive pressure respirator, bag type, manually operated
19IS 6207: 1971Specification for trolleys for oxygen cylinders
20IS 6581: 1972Specification for endotracheal tubes (Rubber)
21IS 6807: 1972Reinforced (Flexo-metallic) Magill’s Endotracheal Tube
22IS 7176: 1985Specification for anaesthetic apparatus, draw over portable type (First Revision)
(1 Revision)
23IS 7409: Part 2: 1994/ISO 5356-2Anaesthetic and respiratory equipment – Conical connectors: Part 2 screw – Threaded weight – Bearing connectors (Second Revision)
(2 Revision)
24IS 7625: 1975Gag, Mouth, Doyen’s Pattern
25IS 7652: 1988Specification for sphygmomanometer, aneroid type (First Revision)
(1 Revision)
26IS 7885: 1985Spray, Macintosh’s Pattern
(1 Revision)
27IS 8254: Part 1: 1976Valve, Non-Rebreathing – Part I: Ruben’s Pattern
28IS 8254: Part 2: 1976Value, Non-rebreathing – Part II : Ambu-Hesse’s Pattern
29IS 8312: 1977Forceps, Introducing, Endotracheal Tube, Magill’s Pattern
30IS 8432: 1977Specification for tubes, tracheostomy (Rubber Or Plastics)
31IS 9462: 1980Specification for humidifier, nebulizing, ventury type
32IS/IEC 80601: Part 2: Sec 30 :2018/IEC 80601-2-30:2018Medical electrical equipment: Part 2 – 30 particular requirements for basic safety and essential performance of automated non – Invasive sphygmomanometers
33IS/ISO 10079 Part 2: 2014/ISO10079-2: 2014Medical Suction Equipment Part 2 Manually Powered Suction Equipment (First Revision)
(1 Revision)
34IS/ISO 10079: Part 3: 2014/ISO 10079-3:2014Medical suction equipment: Part 3 suction equipment powered from a vacuum or positive pressure gas source (First Revision)
(1 Revision)
35IS/ISO 10524 Part 1: 2006/ISO10524-1:2006Pressure Regulators For Use with Medical Gases Part 1 Pressure Regulators and Pressure Regulators with Flow-Metering Devices
36IS/ISO 10524 Part 2: 2005/ISO10524-2:2005Pressure Regulators for use with Medical Gases Part 2 Manifold and Line Pressure Regulators
37IS/ISO 10524: Part 3: 2019/ISO 10524-2:2019Pressure regulators for use with medical gases- Part 3: Pressure regulators integrated with cylinder valves VIPRs First Revision
(1 Revision)
38IS/ISO 10524: Part 4: 2008/ISO 10524 -4:2008Pressure regulators for use with medical gases: Part 4 low – Pressure regulators
39IS/ISO 10651: Part 3: 1997/ISO 10651-3: 1997Lung ventilators for medical use: Part 3 particular requirements for emergency and transport ventilators
40IS/ISO 10651: Part 4: 2002/ISO 10651-4: 2002Lung ventilators for medical use – Particular requirements for basic safety and essential performance: Part 4 particular requirements for operator – Powered resuscitators
41IS/ISO 10651: Part 5: 2006/ISO 10651-5: 2006Lung ventilators for medical use? Particular requirements for basic safety and essential performance: Part 5 gas – Powered emergency resuscitators
42IS/ISO 10651: Part 6: 2004/ISO 10651-6: 2004Lung ventilators for medical use – Particular requirements for basic safety and essential performance: Part 6 home – Care ventilatory support devices
43IS/ISO 11197: 2016/ISO 11197 :2016Medical supply units
44IS/ISO 11712: 2009/ISO 11712 :2009Anaesthetic and respiratory equipment – Supralaryngeal airways and connectors
45IS/ISO 14408: 2005/ISO 14408 :2005Tracheal tubes designed for laser surgery – Requirements for marking and accompanying information
46IS/ISO 15001: 2010/ISO 15001:2010Anaesthetic and respiratory equipment – Compatibility with oxygen (First Revision)
(1 Revision)
47IS/ISO 15002: 2008/ISO15002:2008Flow – Metering devices for connection to terminal units of medical gas pipeline systems
48IS/ISO 16628: 2008/ISO 16628 :2008Tracheobronchial tubes – Sizing and marking
49IS/ISO 26782: 2009/ISO 26782:2009Anaesthetic and respiratory equipment Spirometers intended for the measurement of time-forced expired volumes in humans
50IS/ISO 27427: 2013/ISO 27427:2013Anaesthetic and Respiratory Equipment – Nebulizing Systems and Components
51IS/ISO 5356: Part 1: 2015/ISO 5356-1:2015Anaesthetic and respiratory equipment – Conical connectors: Part 1 cones and sockets (First Revision)
(1 Revision)
52IS/ISO 5356: Part 2: 2012/ISO 5356-2:2015Anaesthetic and respiratory equipment – Conical connectors: Part 2 screw – Threaded weight – Bearing connectors
53IS/ISO 5361: 1999/ISO 5361Anaesthetic and respiratory equipment – Tracheal tubes and connectors
54IS/ISO 5362: 2006/ISO 5362 :2006Anaesthetic reservoir bags
55IS/ISO 5364: 2008/ISO 5364 :2008Anaesthetic and respiratory equipment – Oropharyngeal airways
56IS/ISO 5366: PART 1 :2000/ISO 5366 Part 1: 2000Anaesthetic and respiratory equipment – Tracheostomy tubes: Part 1 tubes and connectors for use in adults
57IS/ISO 5367: 2000/ISO 5367:2000Breathing tubes intended for use with anaesthetic apparatus and ventilators
58IS/ISO 7396: Part 1: 2007Medical gas pipeline systems: Part 1 pipeline systems for compressed medical gases and vacuum
59IS/ISO 7396: Part 2: 2007Medical gas pipelines systems: Part 2 gas scavenging disposal systems
60IS/ISO 81060: Part 1 :2007/IEC81060_1 : 2007Non-Invasive Sphygmomanometers: Part 1 Requirements and Test Methods for non – Automated Measurement Type
61IS/ISO 81060: Part 2: 2018/ISO 81060-2:2018Non-invasive sphygmomanometers – Part 2: Clinical investigation of intermittent automated measurement type
62IS/ISO 9170: PART 1 :2008/ISO 9170-1:2008Terminal units for medical gas pipeline systems: Part 1 terminal units for use with compressed medical gases and vacuum
63IS/ISO 9170: Part 2: 2008/ISO 9170-2:2008Terminal units for medical gas pipeline systems: Part 2 terminal units for anaesthetic gas scavenging systems

Validity Of BIS Certificate For Anaesthetic, Resuscitation, And Allied Equipment

The validity of the BIS Certificate for Medical Electrical Equipment is one year from the date of issuance. After this period, the license can be renewed in the given time; otherwise, a fine of Rs 5000 is imposed.

Timeline For Obtaining For Anaesthetic, Resuscitation, And Allied Equipment

The timeline for obtaining BIS Certification for Medical Electrical Products in India typically ranges from 30 to 40 days. However, this may vary based on the product’s complexity and the application’s completeness.

How Will ELT Corporate Assist You With BIS Certificate for Anaesthetic, Resuscitation, and Allied Equipment?

ELT Corporate delivers full-spectrum support for securing BIS certification for anaesthetic, resuscitation, and allied equipment. We assist at every stage, from the application process and document preparation to liaising with BIS for inspections. Our team ensures ongoing compliance with BIS standards, providing continuous support from initial certification to renewals, ensuring that your certification remains active and uninterrupted.

What Are The Fees Associated With BIS Certification?

The cost of BIS certification varies based on the product category and specific criteria. It typically includes fees for the application, factory inspection, and any necessary testing, depending on the product’s nature and requirements.

Can BIS Certification Be Transferred To Another Manufacturer Or Location?

No, BIS certification is specific to the manufacturer and its production facility. Any changes to the manufacturing setup require a new certification application.

Is BIS Applicable For Medical Devices?

Yes, BIS certification is applicable for medical devices in India. BIS Standards for Medical Devices are designed to ensure that required safety measures are maintained per Indian Standards.

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