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Bouffant Cap - India CDSCO Medical Device Registration

Bouffant Cap is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2023/000211_d27b1b83c0b75038fa9c5eab3e4804bb_fa83831074bbeb7262426f2c01a30a8f. This device is marketed under the brand name FILTRA. The license holder is Thea-Tex Healthcare (India) Private Limited, and it is classified as Device Class Class A. The approving authority is Kokan Division.

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
Bouffant Cap
UID: MFG/MD/2023/000211_d27b1b83c0b75038fa9c5eab3e4804bb_fa83831074bbeb7262426f2c01a30a8f

Brand Name

FILTRA

Device Class

Class A

Approving Authority

Kokan Division

Product Information

Bouffant cap is intended for single use by operating room personnel and other general healthcare workers to protect both patients and healthcare workers against transfer of microorganisms, blood and body fluids, and airborne particulates

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