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Sickle Cell Rapid Test Kit - India CDSCO Medical Device Registration

Sickle Cell Rapid Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000130_6bd7d726e5d497bd9c56b2afe2d814ea_91fa13ece9a601c9ab124b126e22fa69. This device is marketed under the brand name Insta Chikungunya IgG/IgM Rapid Test. The license holder is Seloi Healthcare Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Greater Mumbai 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
Sickle Cell Rapid Test Kit
UID: MFG/IVD/2022/000130_6bd7d726e5d497bd9c56b2afe2d814ea_91fa13ece9a601c9ab124b126e22fa69

Brand Name

Insta Chikungunya IgG/IgM Rapid Test

Device Class

Class B

Approving Authority

Greater Mumbai Division

Product Information

The Sickle Cell Rapid test kit is a lateral flow chromatographic qualitative immunoassay to aid in the rapid diagnosis of sickle cell disorders of hemoglobins A and S using fingerstick or venipuncture whole blood samples. User will be a clinical professional such as a doctor, physician assistant, nurse, clinical or medical assistant, or laboratory technician

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