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EPR Authorization for Cardiology equipment and accessories

Cardiology equipment and accessories

EPR authorization is mandatory for

Cardiology equipment and accessories

Category : EPR Authorization

EEE Code : MDW2

Accessories and equipment for cardiology are vital resources that support the diagnosis, observation, and management of heart-related disorders. Indian Technical Standard MDW2, which outlines specific technical specifications, quality requirements, safety measures, and testing procedures that manufacturers of cardiology equipment and accessories must adhere to, outlines the manufacturing and quality standards for these specialized medical devices in India.

These specifications guarantee that these products are designed, produced, and evaluated in compliance with accepted quality standards. Adhering to these guidelines can help manufacturers gain credibility with healthcare practitioners, as well as open doors for their products in the cutthroat medical equipment industry.

Note: The obligatory EPR Registration Certificate must be obtained by manufacturers who produce cardiac equipment and its components.

The EPR Authorization emphasizes that producers, particularly those who produce cardiology-related medical devices, have an obligation to take proactive steps to ensure appropriate disposal, recycling, and environmentally sound management of their products. This is in line with international initiatives to support ethical and environmentally responsible management of electronic medical equipment, guaranteeing a more secure and long-lasting healthcare environment for everybody.


About Extended Producer Responsibility (EPR) Authorization for E-Waste

An essential program to handle the expanding problem of managing electronic trash, or "e-waste," is called EPRA, or Extended Producer's Responsibility Authorization. Securing EPR authorization from the State Pollution Control Boards (SPCBs) and receiving the EPR Registration Certificate from the Central Pollution Control Board (CPCB) are the two steps in the process of obtaining EPR authorization. With the help of EPRA, manufacturers and importers of electronic goods will take over management of e-waste from consumers and local governments. Electronics importers and manufacturers are obligated by EPRA to assume full responsibility for the whole lifecycle of their products, from manufacturing to disposal. Establishing and financing collection networks, recycling centers, and appropriate e-waste disposal techniques are all part of this. 


Required Documents for Extended Producer Responsibility (EPR) Authorization for E-Waste

  • Address Proof Documents
  • Product Information (including model numbers and production/import history)
  • Valid BIS License
  • CPCB Certification

For more detailed information, please click here.


Registration Process for Extended Producer Responsibility (EPR) Authorization for E-Waste

Step 1: Fill out the application form

Step 2: Attach all the required documents

For more detailed information, please click here


Why Choose Brand Liaison?

Brand Liaison offers valuable assistance in obtaining an EPR Registration Certificate for Cardiology equipment and accessories, Our services include:

  • Expert guidance
  • Streamline process
  • Comprehensive support
  • Cost-effective solutions
  • Time efficient

For a more in-depth understanding of the documentation and procedures involved in obtaining EPR Registration, feel free to connect with our team of experts at +91-9250056788 or +91-8130856678.

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