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Anti-Streptolysin O Test Reagent kit - India CDSCO Medical Device Registration

Anti-Streptolysin O Test Reagent kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000037_f7dd6dca773413aa001bef03e3b93a1f_4c6a2fda0631f6fb01cf27d1a717cad4. This device is marketed under the brand name by UV method. The license holder is Trivitron Healthcare Pvt. Ltd, and it is classified as Device Class Class B. The approving authority is Tamil Nadu.

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
Anti-Streptolysin O Test Reagent kit
UID: MFG/IVD/2020/000037_f7dd6dca773413aa001bef03e3b93a1f_4c6a2fda0631f6fb01cf27d1a717cad4

Brand Name

by UV method

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

ClinReact ITA Anti-Streptolysin O Test Reagent kit (by UV method) is intended for the quantitative determination of Antistreptolysin O (by UV method) in human serum or plasma by spectrophotometry

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