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HIV 1/2 and Syphilis Ab Detection dual test kit - India CDSCO Medical Device Registration

HIV 1/2 and Syphilis Ab Detection dual test kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000109_da7fafecc79bd2cfc96a73a878647da8_a7c32ad147636162ac606208f17d46ba. The license holder is Levram Lifesciences Private Limited, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West Zone.

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 D
HIV 1/2 and Syphilis Ab Detection dual test kit
UID: MFG/IVD/2022/000109_da7fafecc79bd2cfc96a73a878647da8_a7c32ad147636162ac606208f17d46ba

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

The test is for in vitro diagnostic use and intended as an aid to early diagnosis of HIV and Syphilis infection in human serum, Plasma or Whole blood

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