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Sickle Scan Rapid Test - India CDSCO Medical Device Registration

Sickle Scan Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000039_903528de3a3d22cb8d6cc8f2ebcb8c42_0ccbc4f1da413315925a2aafa787630a. This device is marketed under the brand name Sickle SCAN. The license holder is Alpine Biomedicals Private Limited, and it is classified as Device Class Class C. The approving authority is Sub Zonal Baddi.

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 C
Sickle Scan Rapid Test
UID: MFG/IVD/2020/000039_903528de3a3d22cb8d6cc8f2ebcb8c42_0ccbc4f1da413315925a2aafa787630a

Brand Name

Sickle SCAN

Device Class

Class C

Approving Authority

Sub Zonal Baddi

Product Information

SICKLE SCAN rapid test is a lateral flow chromatographic qualitative immunoassay to aid in the rapid diagnosis of sickle cell disorders of haemoglobins A, S, and C 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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