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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_aae3da30aba9fd7c7afe0901310e65ae. 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_aae3da30aba9fd7c7afe0901310e65ae

Brand Name

PTA

Device Class

Class B

Approving Authority

Gujarat

Product Information

Direct-X PTA 0.014โ€ Rx Pre-Dilatation Balloon Catheter

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