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Endotracheal Tube - India CDSCO Medical Device Registration

Endotracheal Tube is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000325_54dca43b6811fc9ced948ca8068b3e81_1208a98dbdbb617d79afd39c6303e944. This device is marketed under the brand name BIP Foley Catheter latex. The license holder is Neon Laboratories Limited, 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
Endotracheal Tube
UID: IMP/MD/2019/000325_54dca43b6811fc9ced948ca8068b3e81_1208a98dbdbb617d79afd39c6303e944

Brand Name

BIP Foley Catheter latex

Device Class

Class B

Approving Authority

CDSCO

Product Information

The BIP Endotracheal Tube is indicated to be used by trained medical staff, for use in airway management by oral or nasal intubation of the patient trachea to create an open airway. The Bactiguardยฎ coating on the BIP Endotracheal Tube has been shown to significantly reduce microbial adhesion

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