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.
Brand Name
Dosi-Flow
License Holder
SURGIPLUSDevice Class
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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