Pure Global

PTCA Catheter - India CDSCO Medical Device Registration

PTCA Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000122_a7d36f5934a191ef9b9439fd936fe51d_ec90e86b4f882b755492c43f4649fd7d. This device is marketed under the brand name MAYA. The license holder is Sahajanand Medical Technologies Limited, and it is classified as Device Class Class D. The approving authority is CDSCO.

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 D
PTCA Catheter
UID: IMP/MD/2022/000122_a7d36f5934a191ef9b9439fd936fe51d_ec90e86b4f882b755492c43f4649fd7d

Brand Name

MAYA

Device Class

Class D

Approving Authority

CDSCO

Product Information

For "Further manufacturing use only" Non-Sterile Device and for Sterile or final Device is indicated for use in the treatment of patients with clinical symptoms of myocardial ischemia related to the pathological condition of one or more coronary arteries. The Maya PTCA catheter is therefore indicated to dilate the diseased segment(MAYA) in a coronary artery or a coronary bypass, to improve myocardial perfusion. It allows also for restoring coronary flow in patients with ST-segment elevation myocardial infarction

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing