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Multi Flow Venturi Mask - India CDSCO Medical Device Registration

Multi Flow Venturi Mask is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000425_a04faa7c6c532609259ad25c0802fff0_05d93d9b619ae3659707d3444377743e. This device is marketed under the brand name HME BVF HME plus BVF. The license holder is DR. RESPIRA CARE PVT LTD, and it is classified as Device Class Class A. 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 A
Multi Flow Venturi Mask
UID: MFG/MD/2022/000425_a04faa7c6c532609259ad25c0802fff0_05d93d9b619ae3659707d3444377743e

Brand Name

HME BVF HME plus BVF

Device Class

Class A

Approving Authority

Gujarat

Product Information

Used when the required concentration needs to change during oxygen therapy, this is done using multiple oxygen dilutor

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