PTCA Catheter
- UID
- IMP/MD/2022/000122_a7d36f5934a191ef9b9439fd936fe51d_ec90e86b4f882b755492c43f4649fd7d
- Device class
- Class D
- Brand name
- MAYA
- License holder
- Sahajanand Medical Technologies Limited
- 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
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.