Pure Global

ALBUMIN TEST REAGENT KIT- BCG method - India CDSCO Medical Device Registration

ALBUMIN TEST REAGENT KIT- BCG method is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000060_dc98f6e1a68f293c73170bf073a8172c_5f79dd327e42285ae6db2d40b18b663c. The license holder is PEERLESS BIOTECH PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is Tamil Nadu.

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
ALBUMIN TEST REAGENT KIT- BCG method
UID: MFG/IVD/2022/000060_dc98f6e1a68f293c73170bf073a8172c_5f79dd327e42285ae6db2d40b18b663c

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

The Albumin test kit is for the quantitative determination of Albumin concentration in human serum or plasma

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing