Pure Global

LEPTOSPIRA IgG/IgM RAPID TEST DEVICE/kit - India CDSCO Medical Device Registration

LEPTOSPIRA IgG/IgM RAPID TEST DEVICE/kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000009_35f8e18af813b0e49369524f264b000c_9b01bf9600cbd4e7ecbf1fdb84a4844d. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class C
LEPTOSPIRA IgG/IgM RAPID TEST DEVICE/kit
UID: MFG/IVD/2021/000009_35f8e18af813b0e49369524f264b000c_9b01bf9600cbd4e7ecbf1fdb84a4844d

Device Class

Class C

Approving Authority

Sub Zonal Baddi

Product Information

For detection of Leptospira in human serum/plasma

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing