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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_a99ec11da76592f8f0d3d91fcd9548a5. 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.

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CDSCO Registered
Class Class C
Ultrasound Equipment
UID: IMP/MD/2021/000713_acf2142af91ade38ef342260ea4df50d_a99ec11da76592f8f0d3d91fcd9548a5

Brand Name

Logiq V2

Device Class

Class C

Approving Authority

CDSCO

Product Information

The device is a general purpose ultrasound system intended for ultrasound imaging, measurement and analysis of the human body for multiple clinical applications including: Ophthalmic; Fetal/OB; Abdominal (Logiq V2); Pediatric; Small Organ (Logiq V2); Neonatal and Adult Cephalic; Cardiac (Logiq V2); Peripheral Vascular; Musculoskeletal Conventional & Superficial; Transrectal; Transvaginal; Transesophageal; Intraoperative (Logiq V2); Thoracic/Pleural for motion and fluid detection and imaging guidance of interventional procedures (Logiq V2).

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