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Erythrocyte sedimentation analyser - India CDSCO Medical Device Registration

Erythrocyte sedimentation analyser is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000206_2ea2c09095e7eb21602f2399875c5e43_8d975fd2e1f03e3c4e3bf00fd8b75579. This device is marketed under the brand name HumaCLIA 150 . The license holder is M/s Stedman Pharmaceuticals Pvt. Ltd., and it is classified as Device Class Class A. 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 A
Erythrocyte sedimentation analyser
UID: IMP/IVD/2019/000206_2ea2c09095e7eb21602f2399875c5e43_8d975fd2e1f03e3c4e3bf00fd8b75579

Brand Name

HumaCLIA 150

Device Class

Class A

Approving Authority

CDSCO

Product Information

HumaSRate 24PT (HumaCLIA 150 ) is a clinical diagnos-tic instrument for determining the sedimentation value of human blood sample

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