PTCA-Percutaneous Transluminal Coronary Angioplasty Catheter - India CDSCO Medical Device Registration

PTCA-Percutaneous Transluminal Coronary Angioplasty Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000385_4abba7cc35a5cca7d38f3541beb5ae1e_a898222f20a1cdf34009a255960dc7c5. This device is marketed under the brand name VEGA. The license holder is Nano Therapeutics Pvt. Ltd., and it is classified as Device Class Class D. The approving authority is CDSCO.

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CDSCO Registered

Class Class D

PTCA-Percutaneous Transluminal Coronary Angioplasty Catheter

UID: IMP/MD/2019/000385_4abba7cc35a5cca7d38f3541beb5ae1e_a898222f20a1cdf34009a255960dc7c5

Brand Name

VEGA

License Holder

Nano Therapeutics Pvt. Ltd.

Device Class

Class D

Approving Authority

CDSCO

Product Information

The Maya Catheter is intended for use in the treatment of patients with clinical symptoms of myocardial symptoms of myocardial ischemia related to the pathological condition of one or more coronary arteries. It is therefore indicated to dilate the diseased segment(VEGA) in a coronary artery or a coronary bypass, to improve myocardial perfusion