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Balloon Inflation Device - India CDSCO Medical Device Registration

Balloon Inflation Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000044_4d5059388d1e93afad1114fa51db4ae2_ba8fe2695f91de3a1e5f1e77b0fb0887. This device is marketed under the brand name FLEXIPORT. The license holder is Invent Biomed Private Limited, 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
Balloon Inflation Device
UID: MFG/MD/2019/000044_4d5059388d1e93afad1114fa51db4ae2_ba8fe2695f91de3a1e5f1e77b0fb0887

Brand Name

FLEXIPORT

Device Class

Class B

Approving Authority

Gujarat

Product Information

Balloon Inflation Device is Precisely design for use during PTCA and any other Intravascular therapeutics that utilize a balloon catheter and pressure monitoring

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