Pure Global

D-DIMER Test Kit - India CDSCO Medical Device Registration

D-DIMER Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000034_80a548620a44c6e83206b941c4619092_27ec4af8e6a7acb8aaf6997ead3acf92. This device is marketed under the brand name Aridia. The license holder is Athenese-Dx Private Limited, and it is classified as Device Class Class C. The approving authority is Central Drug Standard Control Organisation, South Zone.

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
D-DIMER Test Kit
UID: MFG/IVD/2020/000034_80a548620a44c6e83206b941c4619092_27ec4af8e6a7acb8aaf6997ead3acf92

Brand Name

Aridia

Device Class

Class C

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

TRUEchemie D-DIMER is intended for in vitro use as an assayed D-Dimer in serum of laboratory testing procedures for the analytes listed in this package insert

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing