Pure Global

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_d0f19edbde20f91fc06c82614c7a8261. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class C
Endoprosthesis
UID: MFG/MD/2018/000079_4946a93329f923ef34f9cdc2ca91b210_d0f19edbde20f91fc06c82614c7a8261

Brand Name

Nebula

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

Endo Prosthesis are specially used in Femur Neck Fracture. When Femur bone Head is Damaged or Fractured

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing