Pure Global

Urethral Stent - India CDSCO Medical Device Registration

Urethral Stent is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000039_7ef2f19114cd2bd1d408345cba091357_ce8e1718191dfa3be456416d7a24782f. The license holder is Blue Neem Medical Devices Private Limited, and it is classified as Device Class Class C. The approving authority is Sub Zonal Bangalore.

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
Urethral Stent
UID: MFG/MD/2019/000039_7ef2f19114cd2bd1d408345cba091357_ce8e1718191dfa3be456416d7a24782f

Device Class

Class C

Approving Authority

Sub Zonal Bangalore

Product Information

Used for stenting the urethra after hypospedias or epispedias repair and to provide post-operative drainage of the bladder

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing