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Tuberculosis Kit - India CDSCO Medical Device Registration

Tuberculosis Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000143_f410d98cf6a7be4b2a248f27c738cd20_b91a7a190767975dfeb8fc7747da76c8. This device is marketed under the brand name HiMedia. The license holder is HiMedia Laboratories Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Kokan Division.

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
Tuberculosis Kit
UID: MFG/IVD/2023/000143_f410d98cf6a7be4b2a248f27c738cd20_b91a7a190767975dfeb8fc7747da76c8

Brand Name

HiMedia

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Ready prepared slants in glass tubes for maintenance of specimen/ performance of biochemical tests which can can aid in identification of microorganisms

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