CDSCO UID MFG/IVD/2019/000026_c41621073e2937bb997e2a920c961551_762a7ef74f77f253c6c0e107f1234ab4

Diagnostics Test for Syphilis Rapid Test

Name: Diagnostics Test for Syphilis Rapid Test — CDSCO UID MFG/IVD/2019/000026_c41621073e2937bb997e2a920c961551_762a7ef74f77f253c6c0e107f1234ab4
Creator: Nucleus Diagnosys LLP
Keywords: Diagnostics Test for Syphilis Rapid Test, MFG/IVD/2019/000026_c41621073e2937bb997e2a920c961551_762a7ef74f77f253c6c0e107f1234ab4, Device Class Class D, Nucleus Diagnosys LLP, CDSCO registration

Nucleus Diagnosys LLPDevice Class Class DIndia CDSCO

VerifiedCDSCO · official registry

Registration details

UID: MFG/IVD/2019/000026_c41621073e2937bb997e2a920c961551_762a7ef74f77f253c6c0e107f1234ab4
Device class: Class D
License holder: Nucleus Diagnosys LLP
Approving authority: Central Drug Standards Control Organization, Ahmedabad
Product information: Syphilis test reagents/kits is a medical device intended for the screening of Syphilis in blood/body fluids

About this record

Diagnostics Test for Syphilis Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000026_c41621073e2937bb997e2a920c961551_762a7ef74f77f253c6c0e107f1234ab4. The license holder is Nucleus Diagnosys LLP, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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