Leishmania Ab Rapid Test - India CDSCO Medical Device Registration

Leishmania Ab Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000088_99594fc3515a04388b5c9638d81ee02c_435e67ce258d03c1e53c20aa1c27b813. This device is marketed under the brand name HaemNest Sheath Fluid. The license holder is Genenest Biotech Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Uttar Pradesh.

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CDSCO Registered

Class Class B

Leishmania Ab Rapid Test

UID: MFG/IVD/2022/000088_99594fc3515a04388b5c9638d81ee02c_435e67ce258d03c1e53c20aa1c27b813

Brand Name

HaemNest Sheath Fluid

License Holder

Genenest Biotech Pvt. Ltd.

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

The Leishmania Ab Rapid Test (HaemNest Sheath Fluid) is a rapidchromatographic immunoassay for thequalitative detection of igG and igMantibodies to Leishmania in human's wholeblood, serum or plasma

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Lyse LB (HaemNest Lyse LB )

Brand: HaemNest Sheath Fluid

Genenest Biotech Pvt. Ltd.

Leishmania Ab Rapid Test - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

DJ Fang

Lyse LB (HaemNest Lyse LB )

Lyse reagent

Lyse reagent

Ferritin

Scrub Typhus Ab Rapid Test

Diluent (HaemNest Diluent )

Cleaners Reagent

Cleaners Reagent

Cleaners Reagent

Cleaners Reagent

Lyse LB (HaemNest Lyse LB )

Lyse reagent

Lyse reagent

Ferritin

Scrub Typhus Ab Rapid Test

Diluent (HaemNest Diluent )

Cleaners Reagent

Cleaners Reagent

Cleaners Reagent

Cleaners Reagent