CDSCO Medical Device Registration for Pacemaker - Process, Documentation, Benefits acquired


Updated on July 06, 2024 06:14:04 PM

CDSCO stands for The Central Drugs Standard and Control Organisation. It is India's National Regulatory Authority (NRA) for Cosmetics, Pharmaceuticals and Medical Devices, being a highly powerful organization of India.


Within the CDSCO, the Drug Controller General of India (DCGI) regulates Pharmaceuticals & Medical Devices and its positioning with the Ministry of Health and Family Welfare Under Drugs and Cosmetics Act 1940 and Rules 1945.

CDSCO Medical Device Registration for Bone Marrow Cell Separator - Process, Importance, Fee

What is a Pacemaker as a Medical Device?

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A Pacemaker is a battery-powered small device that helps in preventing the neart from beating too slowly A Pacemaker is also known as a Cardiac Pacing Device which is the size of a matchbox.

There are various types of Pacemakers: Single Chamber Pacemaker. Dual Chamber Pacemaker and Biventricular Pacemaker. The primary purpose of a pacemaker is to maintain an adequate heart rate.

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What is CDSCO Medical Device Registration for Pacemakers?

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The indian govemment has announced its plan to bring al the Vedical Devices including Implants and Contraceptives under the review of the Central Drugs Standard Control Organisation.

CDSCO Medical Device Registration for Pacemakers is a process of ontaining approval from the regulatory authority to ensure the efficiency and quality of Pharmaceuticals Medical Devices and Cosmetics.

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Procedure of doing CDSCO Medical Device Registration for Pacemaker

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Following steps can be followed for doing CDSCO Medical Device for Pacemaker.

Step 1 : Online Registration

To apply for CDSCO Registration you need to visit the official website of CDSCO. Open the ‘CDSCO SUGAM Portal’ then Click on the ‘SIGN UP HERE’ option.

Step 2 : Filling up the details

The Registration form is divided into two parts, ‘Applicant Details’- the applicant needs to submit his/her personal details, ‘Registered Indian Address'- the applicant needs to submit his/her organization's details.

Step 3 : Document Submission

Complete the application process by submitting the required documents for the verification process.

Step 4 : Verification of the Registration

To verify the registration,a confirmation link will be sent to the registered email Id. By clicking on the link, it will activate your account on the SUGAM portal.

Step 5 : Approval from Authority

After Clicking on the confirmation, the registration application will be sent to the concerned authority for approval. If the application got approved by the CDSCO Officials, an email of approval will be sent to the registered email Id, vice versa for the case of rejection.

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Benefits acquired after CDSCO Registration for Pacemaker

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The benefits acquired after CDSCO registration for Pacemaker can be seen as follows :

  • * Ensuring Safety : The main aim of the Central Drugs Standard Control Organisation is to safeguard public health. The quality and efficiency of the device or product goes under a verification process done by the CDSCO officials The safety and health issues of certain types of equipment are not a concern with registered Medical Devices as a finished product.
  • Regulatory Compliance : CDSCO Registration provides Regulatory Compliance referring to a procedure of foliowing relevant laws and regulations CDSCO ensures that the Medical Devices that are used by the public are meeting the safety and quality standards set by CDSCO.
  • Safeguard Public Health : COSCO is constantly striving to aing out transparency.

accountability, and uniformity in its services in order to ensure safety efficacy and quality of medical devices manufactured, imported, and distributed in the country. The main joo and objective of CDSCO is to safeguard Public Health

Benefits for Bone Marrow Cell
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CDSCO Fee for Product

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The Professional Fee For CDSCO import Certificate for Cosmetic products is INR 99,999/- only with Cokion.

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Documents required in CDSCO Registration for Pacemaker as a Medical Device

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Important documents required in the process are as follows :

Documents Required

  • Application form MD 7.
  • Challan TR6
  • ISO 13485
  • Power of Attorney
  • An Undertaking stating that only accurate information is provided
  • Certificate of quality assurance
  • Declaration of conformity
  • Master Plant File
  • Device Master File
  • FSC
Medical Devices
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Conclusion

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CDSCO registration is required for all kinds of Medical Devices as they contains a risk level. There has definitely been significant market growth in the medical device industry because of vanous factors, which is a necessary and profitable domain for the country. As the Indian government nas announced its plan to bring all Medical Devices under a review of CDSCD thus it is important to complete the registration process on the official website of CDSCO

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