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Pre-Dilatation Balloon Catheter - India CDSCO Medical Device Registration

Pre-Dilatation Balloon Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2018/000101_ac600c046cd72b56a5a05287dc51e57e_12b51ed0ae974c5fdd72b07b05725f75. This device is marketed under the brand name PTA. The license holder is MIV Therapeutics (India) Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Gujarat.

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 B
Pre-Dilatation Balloon Catheter
UID: MFG/MD/2018/000101_ac600c046cd72b56a5a05287dc51e57e_12b51ed0ae974c5fdd72b07b05725f75

Brand Name

PTA

Device Class

Class B

Approving Authority

Gujarat

Product Information

PTA Pre Dilatation Catheter is intended for dilatation of lesions in the iliac, femoral, popliteal, infrapopliteal, and renal arteries)

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