Pure Global

Ultrasound Equipment - India CDSCO Medical Device Registration

Ultrasound Equipment is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000713_acf2142af91ade38ef342260ea4df50d_2e0acbdfe3187d16fb983d58ebae4c27. This device is marketed under the brand name Logiq V2. The license holder is Wipro GE Healthcare Private Limited, and it is classified as Device Class Class C. 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 C
Ultrasound Equipment
UID: IMP/MD/2021/000713_acf2142af91ade38ef342260ea4df50d_2e0acbdfe3187d16fb983d58ebae4c27

Brand Name

Logiq V2

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Versana Active is a general purpose diagnostic ultrasound system intended for use by qualified and trained healthcare professionals for ultrasound imaging, measurement, display and analysis of the human body and fluid. Versana Active clinical applications include: Fetal/Obstetrics, Abdominal (Logiq V2), Pediatric, Small Organ (Logiq V2), Neonatal Cephalic, Adult Cephalic, Cardiac (includes Adult and Pediatric, Peripheral Vascular, Musculoskeletal Conventional, Musculoskeletal Superficial, Thoracic/Pleural, Transcranial, Transrectal, Transvaginal, and Tissue Biopsy/Fluid Drainage. Versana Active ultrasound system is not intended for ophthalmic use or any use causing the acoustic beam to pass through the eye

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing