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Magnesium Reagent Test Kit - India CDSCO Medical Device Registration

Magnesium Reagent Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000008_ea8b198acffc35b8196df96cb44778b4_0d671100d0d025c6da99ff900c8555c5. This device is marketed under the brand name ARSENAZO METHOD. The license holder is BIOLINE DIAGNOSTICS LLP, and it is classified as Device Class Class B. The approving authority is North 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
Magnesium Reagent Test Kit
UID: MFG/IVD/2019/000008_ea8b198acffc35b8196df96cb44778b4_0d671100d0d025c6da99ff900c8555c5

Brand Name

ARSENAZO METHOD

Device Class

Class B

Approving Authority

North West Delhi Division

Product Information

Magnesium is a stable two liquid reagent used for in-vitro diagnosis of Magnesium present in human serum / plasma / Urine and CSF

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