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RF- Latex Agglutination kit - India CDSCO Medical Device Registration

RF- Latex Agglutination kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000034_76e889a89e0b1f1552a4b4dc0048670b_6ffe2d850fc79f82d15823807b9227b3. The license holder is ADI Diagnostics Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Telangana.

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CDSCO Registered
Class Class B
RF- Latex Agglutination kit
UID: MFG/IVD/2019/000034_76e889a89e0b1f1552a4b4dc0048670b_6ffe2d850fc79f82d15823807b9227b3

Device Class

Class B

Approving Authority

Telangana

Product Information

For the qualitative and semi-quantitative measurement of RF in human serum

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