Pure Global

BLOOD CELL DILUENT KIT - India CDSCO Medical Device Registration

BLOOD CELL DILUENT KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000077_a78c0aa7ef3447ea9d31430a4c5a209a_6877cf2a3dbde7149944678727909ea7. This device is marketed under the brand name RECOMBIGEN. The license holder is RECOMBIGEN LABORATORIES PVT. LTD, and it is classified as Device Class Class B. The approving authority is North West Delhi 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
BLOOD CELL DILUENT KIT
UID: MFG/MD/2019/000077_a78c0aa7ef3447ea9d31430a4c5a209a_6877cf2a3dbde7149944678727909ea7

Brand Name

RECOMBIGEN

Device Class

Class B

Approving Authority

North West Delhi Division

Product Information

This kit is designed for health Services Laboratories for suspension and preservation of human red blood cells for use in in vitro immunohematology tests. The mixture is intended for professional use.

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing