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Diagnostics test reagent kits for C-reactive protein latex - India CDSCO Medical Device Registration

Diagnostics test reagent kits for C-reactive protein latex is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000130_3a0586b5a2e6fafe7f9b21e12524d598_b5539fa585f249fe0726fa6c9b0c10f6. 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 C-reactive protein latex
UID: MFG/IVD/2021/000130_3a0586b5a2e6fafe7f9b21e12524d598_b5539fa585f249fe0726fa6c9b0c10f6

Brand Name

IgM

Device Class

Class B

Approving Authority

Greater Mumbai Division

Product Information

C-reactive protein (IgM) tests Reagent / kits is medical device intended for estimation C-reactive protein (IgM) Serum

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