RPR Antigen Test - India CDSCO Medical Device Registration

RPR Antigen Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000041_a95cee803d3e47f1bcb0db36e5b52cb9_d3f0914847510c4c5b5a4933c5326da2. This device is marketed under the brand name TurbiMAX & OEM. The license holder is Avecon Healthcare Pvt. Ltd, and it is classified as Device Class Class C. The approving authority is Sub Zonal Baddi.

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 C

RPR Antigen Test

UID: MFG/IVD/2019/000041_a95cee803d3e47f1bcb0db36e5b52cb9_d3f0914847510c4c5b5a4933c5326da2

Brand Name

TurbiMAX & OEM

License Holder

Avecon Healthcare Pvt. Ltd

Device Class

Class C

Approving Authority

Sub Zonal Baddi

Product Information

Reagent kit for the qualitative and semi quantitative determination of Rapid Plasma Reagin in Human Serum / Plasma

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