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TOXOPLASMA GONDII RAPID TEST DEVICE/Kit - India CDSCO Medical Device Registration

TOXOPLASMA GONDII RAPID TEST DEVICE/Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000009_6c137a28e709a2c2bc7297d6334042e6_f4c73e0c847baadc159b05812afee4da. The license holder is Sidak Lifecare Pvt Ltd, and it is classified as Device Class Class C. The approving authority is Sub Zonal Baddi.

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 C
TOXOPLASMA GONDII RAPID TEST DEVICE/Kit
UID: MFG/IVD/2021/000009_6c137a28e709a2c2bc7297d6334042e6_f4c73e0c847baadc159b05812afee4da

Device Class

Class C

Approving Authority

Sub Zonal Baddi

Product Information

For detection of toxoplasma gondii

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