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Sickle Cell Assay Kit - India CDSCO Medical Device Registration

Sickle Cell Assay Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000096_eb738ee6ecb59087ff7b6add0d57e574_fbd1360f71dac499102df0b57cda3a87. This device is marketed under the brand name ADA. The license holder is Lab-Care Diagnostics (India) Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Gujarat.

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 Assay Kit
UID: MFG/IVD/2021/000096_eb738ee6ecb59087ff7b6add0d57e574_fbd1360f71dac499102df0b57cda3a87

Brand Name

ADA

Device Class

Class B

Approving Authority

Gujarat

Product Information

Sickle Cell Assay Kit (ADA) is a qualitative solubility test kit for testing for the presence of sickling hemoglobin in human blood or sickle cell control material. This is a simple and stable screening test and so samples tested positive should be confirmed by electrophoresis so as to reduce the chances of false positives

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