Pure Global

Diagnostic Ultrasound - India CDSCO Medical Device Registration

Diagnostic Ultrasound is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000350_c5aa46834002b613920a81dfd666003d_ef4c043411e3232fbea36fa12ac3c2a3. This device is marketed under the brand name Acclarix AX3/ Aeroscan CD10 Pro. The license holder is KONICA MINOLTA HEALTHCARE INDIA PRIVATE LIMITED, and it is classified as Device Class Class B. 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
Powered by Pure Global AI
CDSCO Registered
Class Class B
Diagnostic Ultrasound
UID: IMP/MD/2023/000350_c5aa46834002b613920a81dfd666003d_ef4c043411e3232fbea36fa12ac3c2a3

Brand Name

Acclarix AX3/ Aeroscan CD10 Pro

Device Class

Class B

Approving Authority

CDSCO

Product Information

Acclarix LX3 series Diagnostic Ultrasound System is intended for use by a qualified physician or allied health professional for ultrasound evaluations in hospital and clinics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing