Immunofluorescence Analyzer - India CDSCO Medical Device Registration

Immunofluorescence Analyzer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000248_4a4f086c647d2fdfedcc27ce352a2b8f_265932ce371620e2c6217e24ecc30ca1. This device is marketed under the brand name AURA Fia Immunofluorescence Analyzer. The license holder is INDO-MIM TEC PRIVATE LIMITED, and it is classified as Device Class Class A. The approving authority is CDSCO.

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

CDSCO Registered

Class Class A

Immunofluorescence Analyzer

UID: IMP/IVD/2022/000248_4a4f086c647d2fdfedcc27ce352a2b8f_265932ce371620e2c6217e24ecc30ca1

Brand Name

AURA Fia Immunofluorescence Analyzer

License Holder

INDO-MIM TEC PRIVATE LIMITED

Device Class

Class A

Approving Authority

CDSCO

Product Information

The Immunofluorescence Analyzer and Test Device are both for in vitro diagnostic use only. This analyzer is suitable for laboratories with professional testing ability in medical institutions, such as central laboratory, emergency laboratory, clinical departments and physical examination center.