Rapid Plasma Reagin Card Test for Syphilis - India CDSCO Medical Device Registration

Rapid Plasma Reagin Card Test for Syphilis is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000086_816fbb6e931f208f7a5f9f1f47b3ef75_661095144420c835fc8fc2f1ee1714d5. This device is marketed under the brand name RPR. The license holder is CORAL CLINICAL SYSTEMS A DIVISION OF TULIP DIAGNOSTICS PRIVATE LIMITED, and it is classified as Device Class Class D. The approving authority is CDSCO -North Zone, Ghaziabad.

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CDSCO Registered

Class Class D

Rapid Plasma Reagin Card Test for Syphilis

UID: MFG/IVD/2021/000086_816fbb6e931f208f7a5f9f1f47b3ef75_661095144420c835fc8fc2f1ee1714d5

Brand Name

RPR

License Holder

CORAL CLINICAL SYSTEMS A DIVISION OF TULIP DIAGNOSTICS PRIVATE LIMITED

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

The Rapid Plasma Reagin (RPR)/ Carbon Antigen test is a macroscopic non Treponemal flocculation test for the detection and quantitation of antilipoidal antibodies. Non Treponemal tests like CARBOGEN are of great value when used for Syphilis screening and follow up of therapy