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Rubella IgG/Igm Rapid Test - India CDSCO Medical Device Registration

Rubella IgG/Igm Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000109_f8dcb7d0ded506b0a462ad826e2e15e4_39100645108f32cd4cc1b3a1058d3d1d. 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.

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 B
Rubella IgG/Igm Rapid Test
UID: MFG/IVD/2021/000109_f8dcb7d0ded506b0a462ad826e2e15e4_39100645108f32cd4cc1b3a1058d3d1d

Brand Name

3 Parameters

Device Class

Class B

Approving Authority

West Delhi Division

Product Information

The Rubella IgG/lgM kit is a rapid, qualitative and differential test for the detection of antibodies to Rubella virus (3 Parameters) in human serum or plasma. This test is intended for use as an indicator of immune status or for confirmation of recent Rubella infection

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