Pure Global

Esophageal Balloon Catheter - India CDSCO Medical Device Registration

Esophageal Balloon Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000312_ba6191c09dd9faf958ff23df65274945_993d89f6e19a01f8e7936857d66049bd. This device is marketed under the brand name Endoline. The license holder is ENDOLINE PROSCOPE SYSTEMS, and it is classified as Device Class Class B. The approving authority is Uttar Pradesh.

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 B
Esophageal Balloon Catheter
UID: MFG/MD/2022/000312_ba6191c09dd9faf958ff23df65274945_993d89f6e19a01f8e7936857d66049bd

Brand Name

Endoline

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

The balloon dilatation catheter is indicated for balloon dilatation of Esophagus /Colon due to Achalasia for the purpose to dilate muscle fibers

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing