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Endoprosthesis - India CDSCO Medical Device Registration

Endoprosthesis is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2018/000079_4946a93329f923ef34f9cdc2ca91b210_e2ae56dda4cc2ef2f45c5daf0eb80ed7. This device is marketed under the brand name Nebula. The license holder is Nebula Surgical Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class C
Endoprosthesis
UID: MFG/MD/2018/000079_4946a93329f923ef34f9cdc2ca91b210_e2ae56dda4cc2ef2f45c5daf0eb80ed7

Brand Name

Nebula

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

Endoprosthesis is a procedure for replacing a joint in the body that has lost its functionality either through injury or disease in part or whole with an implant. It is a condition in which joint functionality is significantly damaged, or the joint is a source of severe pain

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