Sickle Cell Rapid Test
- UID
- MFG/IVD/2023/000145_578a3211bbb7984d85c0620e03405a7e_bbcdd676ac44e9079a4d585adc65b05e
- Device class
- Class B
- Brand name
- SickleCatch™
- License holder
- Mylab Discovery Solutions Pvt. Ltd.
- Approving authority
- Kokan Division
- Product information
- Sickle cell rapid test is lateral flow immuno-chromatographic qualitative assay to aid in rapid diagnosis of sickle cell disorder of hemoglobin A, S and C using whole blood sample (SickleCatch™) to screen individuals of any age (SickleCatch™), including newborns. This In-vitro diagnostic test intended to be used by healthcare professionals
Sickle Cell Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000145_578a3211bbb7984d85c0620e03405a7e_bbcdd676ac44e9079a4d585adc65b05e. This device is marketed under the brand name SickleCatch™. The license holder is Mylab Discovery Solutions Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Kokan Division.
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