Pure Global

Sauton’s Fluid Medium Base - India CDSCO Medical Device Registration

Sauton’s Fluid Medium Base is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000143_e61ee2312a45254bad52fb37121aa6bf_4316cbc89d6f638abefe8328a8313f82. This device is marketed under the brand name HiMedia. The license holder is HiMedia Laboratories Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Kokan Division.

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
Sauton’s Fluid Medium Base
UID: MFG/IVD/2023/000143_e61ee2312a45254bad52fb37121aa6bf_4316cbc89d6f638abefe8328a8313f82

Brand Name

HiMedia

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Recommended for cultivation and enumeration of Mycobacteria, in accordance with IP

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing