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GAUZE - India CDSCO Medical Device Registration

GAUZE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000357_3f60ac4a0197be06aedc23bfd0f74513_5204848b4f10d529074b6b474a8ceda1. This device is marketed under the brand name SCHEDULE F II. The license holder is M/s JAYCOT INDUSTRIES, and it is classified as Device Class Class B. The approving authority is Telangana.

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
GAUZE
UID: MFG/MD/2022/000357_3f60ac4a0197be06aedc23bfd0f74513_5204848b4f10d529074b6b474a8ceda1

Brand Name

SCHEDULE F II

License Holder

M/s JAYCOT INDUSTRIES

Device Class

Class B

Approving Authority

Telangana

Product Information

Used for medical purposes in hospitals, nursing homes, dispensaries and at home (SCHEDULE F II) etc. because of its property of high fluid absorbency.

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