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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.

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CDSCO Registered
Class Class D
PTCA Balloon Catheter
UID: MFG/MD/2019/000110_35f2171fa613585bd5d0311eff170695_2ad5ab251353e752c5a48a1ed0897db5

Brand Name

Ripper, Vector Pro, Impeller, Waive

Device Class

Class D

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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