CDSCO UID MFG/IVD/2021/000109_99594fc3515a04388b5c9638d81ee02c_52924ebc1857b59b0771b47591a58dd5

Leishmania Ab Rapid Test

Biotrol Laboratories Pvt. Ltd.·Device Class Class B·India CDSCO·Brand: 3 Parameters
Registration details
UID
MFG/IVD/2021/000109_99594fc3515a04388b5c9638d81ee02c_52924ebc1857b59b0771b47591a58dd5
Device class
Class B
Brand name
3 Parameters
Approving authority
West Delhi Division
Product information
The Leishmania Ab Rapid Test is a lateral flow immunoassay for the qualitative detection of the antibodies specific to leishmanial speciies (3 Parameters), the visceral leishmaniasis causative protozoans in human serum, plasma and whole blood. It is intended to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of the disease of visceral leishmaniasis
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About this record

Leishmania Ab Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000109_99594fc3515a04388b5c9638d81ee02c_52924ebc1857b59b0771b47591a58dd5. This device is marketed under the brand name 3 Parameters. The license holder is Biotrol Laboratories Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is West Delhi Division.

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