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Ferritin Rapid Quantitative Test - India CDSCO Medical Device Registration

Ferritin Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000395_4691badd306e7d777ac9f907c8fccd61_235ab10ae778e80ee00895c306d49a0a. This device is marketed under the brand name Biotime . The license holder is M/s Vishat Diagnostic Pvt Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.

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
Ferritin Rapid Quantitative Test
UID: IMP/IVD/2021/000395_4691badd306e7d777ac9f907c8fccd61_235ab10ae778e80ee00895c306d49a0a

Brand Name

Biotime

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Biotime Ferritin Rapid Quantitative Test is intended to quantify the concentration of ferritin in human serum on Biotime FIA Analyzers by fluorescent immunoassay. The test is used as an aid detection of anemia

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