PTCA Balloon Catheter - India CDSCO Medical Device Registration
PTCA Balloon Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000110_35f2171fa613585bd5d0311eff170695_2ad5ab251353e752c5a48a1ed0897db5. This device is marketed under the brand name Ripper, Vector Pro, Impeller, Waive. The license holder is Sahajanand Laser Technology Limited (SLTL Medical), and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, Ahmedabad.
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.
Brand Name
Ripper, Vector Pro, Impeller, Waive
License Holder
Sahajanand Laser Technology Limited (SLTL Medical)Device Class
Approving Authority
Central Drug Standards Control Organization, Ahmedabad
Product Information
PTCA Balloon Catheter is intended to be used for Percutaneous Transluminal Coronary Angioplasty (Ripper, Vector Pro, Impeller, Waive) for the purpose of improving myocardial blood flow in the localized stenotic lesions of coronary arteries
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