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I.V. Flow Regulator - India CDSCO Medical Device Registration

I.V. Flow Regulator is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000336_49a4a9a5c46816539d0d1912ceae39c0_aac755cf7ae68d4d2b464ce44a96aa77. This device is marketed under the brand name Dosi-Flow. The license holder is SURGIPLUS, and it is classified as Device Class Class B. The approving authority is CDSCO.

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
I.V. Flow Regulator
UID: IMP/MD/2019/000336_49a4a9a5c46816539d0d1912ceae39c0_aac755cf7ae68d4d2b464ce44a96aa77

Brand Name

Dosi-Flow

License Holder

SURGIPLUS

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Flow regulator is indicated for gravity feed intravenous infusion of parenteral solutions, allowing selection of a determinated flow rate (Dosi-Flow), which must be verified through a drip chamber.

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