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Tracheostomy Inner Cannula - India CDSCO Medical Device Registration

Tracheostomy Inner Cannula is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000367_857eb793e21f97738590cd4202e92f05_cc3da0f81c9897886440fb13ccd1f23b. This device is marketed under the brand name Portex® BLUselect® Suctionaid® . The license holder is Smiths Medical India Private 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
Tracheostomy Inner Cannula
UID: IMP/MD/2020/000367_857eb793e21f97738590cd4202e92f05_cc3da0f81c9897886440fb13ccd1f23b

Brand Name

Portex® BLUselect® Suctionaid®

Device Class

Class B

Approving Authority

CDSCO

Product Information

The BLUselect® Inner Cannula is intended to be used with the Smiths Medical Portex® BLUselect® Tracheostomy Tube for patients that require an artificial airway due to trauma or medical condition. Maximum recommended period of use is 29 days.

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