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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/2018/000263_54dca43b6811fc9ced948ca8068b3e81_971e548515ea16906913b07a610329c4. This device is marketed under the brand name Portex. The license holder is Smiths Medical India Pvt Ltd, 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/2018/000263_54dca43b6811fc9ced948ca8068b3e81_971e548515ea16906913b07a610329c4

Brand Name

Portex

Device Class

Class B

Approving Authority

CDSCO

Product Information

It is intended for oral and/or nasal intubation for airway management. Expert clinical judgement should be exercised in the selection of the appropriate tracheal tube and style for an individual patient.

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