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Endobronchial Tube - India CDSCO Medical Device Registration

Endobronchial Tube is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000612_52e13cf2a5c0ac558b9ae7c209bb8dc8_7535132afd43f174f97387ada24d4e90. This device is marketed under the brand name TUOREN. The license holder is TUOREN MEDICAL DEVICE INDIA PVT. LTD., and it is classified as Device Class Class B. The approving authority is Haryana.

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
Endobronchial Tube
UID: MFG/MD/2022/000612_52e13cf2a5c0ac558b9ae7c209bb8dc8_7535132afd43f174f97387ada24d4e90

Brand Name

TUOREN

Device Class

Class B

Approving Authority

Haryana

Product Information

The Endobronchial Tube is used to isolate the left or the right lung of a patient for surgery, one lung ventilation or one lung anaesthesia

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