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Immunofluorescence Analyzer - India CDSCO Medical Device Registration

Immunofluorescence Analyzer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000457_4a4f086c647d2fdfedcc27ce352a2b8f_7811c09738706c6b0f7cdec211dca579. This device is marketed under the brand name Eoscare. The license holder is M/S CLEAR IMAGING MEDICAL SYSTEM 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
Immunofluorescence Analyzer
UID: IMP/IVD/2022/000457_4a4f086c647d2fdfedcc27ce352a2b8f_7811c09738706c6b0f7cdec211dca579

Brand Name

Eoscare

Device Class

Class A

Approving Authority

CDSCO

Product Information

The Immunofluorescence Analyzer should be used together with immunofluorescence detection reagents

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