Pure Global

FOLEY BALLOON CATHETER 3 WAY - India CDSCO Medical Device Registration

FOLEY BALLOON CATHETER 3 WAY is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2023/000174_d2b8c72ff278af80cde5d4730d5ee352_4b7eb6fcdc2fd39bbecf1f809164f39f. This device is marketed under the brand name ASCO. The license holder is STERIMED SURGICALS (INDIA) PVT. LTD., and it is classified as Device Class Class B. The approving authority is Haryana.

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
FOLEY BALLOON CATHETER 3 WAY
UID: MFG/MD/2023/000174_d2b8c72ff278af80cde5d4730d5ee352_4b7eb6fcdc2fd39bbecf1f809164f39f

Brand Name

ASCO

Device Class

Class B

Approving Authority

Haryana

Product Information

A long, small gauge catheter designed for insertion directly into a ureter, either through the urethra and bladder or post eriorly via the Kidney.

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing