Pure Global

Partial Ossicular Replacement Prosthesis - India CDSCO Medical Device Registration

Partial Ossicular Replacement Prosthesis is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000481_006693e75909682a2a401e0750d86283_aaa80c0492eb0b16ff7409349ca829e8. This device is marketed under the brand name myringotomy. The license holder is EON MEDITECH PRIVATE LIMITED, 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
Partial Ossicular Replacement Prosthesis
UID: MFG/MD/2022/000481_006693e75909682a2a401e0750d86283_aaa80c0492eb0b16ff7409349ca829e8

Brand Name

myringotomy

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

PORP replaces only the incus and malleus (myringotomy) to connect Tympanic Membrane and Head of the stapes

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing