TB/NTM PCR Kit [883003W/E]
- UID
- IMP/IVD/2021/000418_1bc5deda6f8c4bf7798a181a74436511_f299c2816cadb9d352da5d19c2e73fc5
- Device class
- Class C
- Brand name
- LyteStar TB/NTM PCR Kit 3.0
- License holder
- ADT India Pvt. Ltd.
- Approving authority
- CDSCO
- Product information
- The LyteStar™ TB/NTM PCR Kit 3.0 is intended for specific detection of Mycobacterium tuberculosis complex (LyteStar TB/NTM PCR Kit 3.0) and non-tuberculos mycobacteria (LyteStar TB/NTM PCR Kit 3.0) from human sputum, bronchial washings, cerebrospinal fluid (LyteStar TB/NTM PCR Kit 3.0), urine, body fluids, tissue and EDTA-whole blood
TB/NTM PCR Kit [883003W/E] is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000418_1bc5deda6f8c4bf7798a181a74436511_f299c2816cadb9d352da5d19c2e73fc5. This device is marketed under the brand name LyteStar TB/NTM PCR Kit 3.0. The license holder is ADT India Pvt. Ltd., and it is classified as Device Class Class C. 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.