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Diagnostics test reagent kits for WIDAL - India CDSCO Medical Device Registration

Diagnostics test reagent kits for WIDAL is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000130_ae4788f2bd637dc6a671b91ef1aa971c_497a70216bf85d4febb1be8264045651. This device is marketed under the brand name IgM. The license holder is Vimek Bioconcept Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Greater Mumbai 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
Diagnostics test reagent kits for WIDAL
UID: MFG/IVD/2021/000130_ae4788f2bd637dc6a671b91ef1aa971c_497a70216bf85d4febb1be8264045651

Brand Name

IgM

Device Class

Class B

Approving Authority

Greater Mumbai Division

Product Information

Widal test for the qualitative and semi-quantitative determination of Widal Antibodies in serum

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