Pure Global

Leptospira Rapid Test Kit - India CDSCO Medical Device Registration

Leptospira Rapid Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000001_fe64a6640e36a02de33b961dd75aa4fe_787d1bfb5d4eadaf6c34bd5c6aa5e29e. The license holder is M/S. MEDSOURCE OZONE BIOMEDICALS PVT LTD, and it is classified as Device Class Class B. The approving authority is Haryana.

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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
Leptospira Rapid Test Kit
UID: MFG/IVD/2020/000001_fe64a6640e36a02de33b961dd75aa4fe_787d1bfb5d4eadaf6c34bd5c6aa5e29e

Device Class

Class B

Approving Authority

Haryana

Product Information

Rapid immunochromatographic assay for qualitative detection of antibodies (NA) to LEPTOSPIRA INTEROGANS in human serum/ plasma. It is intended to be used as a screening test

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing