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Syphilis ELISA Kit - India CDSCO Medical Device Registration

Syphilis ELISA Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000004_7e39b2dbc33ab502ea7bb0c152682d27_fb3a446e781d0a0adf5dd29ffaf76a1d. The license holder is KARWA ENTERPRISES PRIVATE LIMITED, and it is classified as Device Class Class D. The approving authority is CDSCO -North Zone, Ghaziabad.

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
Syphilis ELISA Kit
UID: MFG/IVD/2020/000004_7e39b2dbc33ab502ea7bb0c152682d27_fb3a446e781d0a0adf5dd29ffaf76a1d

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

Test kit for Detection of Syphilis

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