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Chikungunya lgM/lgG Rapid Test-Sheet - India CDSCO Medical Device Registration

Chikungunya lgM/lgG Rapid Test-Sheet is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000111_2371763717ad44f87fa1f33c77dc05aa_cdab5dd1c37e89474502ddf792c8ef35. This device is marketed under the brand name Mediline-SA. The license holder is S.A-MEDLINE PRIVATE LIMITED, and it is classified as Device Class Class C. The approving authority is CDSCO -North Zone, Ghaziabad.

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CDSCO Registered
Class Class C
Chikungunya lgM/lgG Rapid Test-Sheet
UID: MFG/IVD/2023/000111_2371763717ad44f87fa1f33c77dc05aa_cdab5dd1c37e89474502ddf792c8ef35

Brand Name

Mediline-SA

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

The Chikungunya lgM/lgG Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of lgM/lgG anti-chikungunya virus (Mediline-SA) in human serum, plasma or whole blood. It is intended to be used as a screening test and as an aid in the diagnosis of infection with CHIK. Any reactive specimen with the Chikungunya lgM/lgG Rapid Test must be confirmed with alternative testing method(Mediline-SA) and clinical findings

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