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Ultrasound System - India CDSCO Medical Device Registration

Ultrasound System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000179_3a9c379a2b7d40000a6f431e218b71a8_9343d4564ecbdabe8860b57e497674e1. This device is marketed under the brand name LOGIQ P9. The license holder is Wipro GE Medical Device Manufacturing Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is Sub Zonal Bangalore.

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 System
UID: MFG/MD/2022/000179_3a9c379a2b7d40000a6f431e218b71a8_9343d4564ecbdabe8860b57e497674e1

Brand Name

LOGIQ P9

Device Class

Class C

Approving Authority

Sub Zonal Bangalore

Product Information

LOGIQ P9 Diagnostic Ultrasound Imaging System (LOGIQ P9) is general healthcare purpose ultrasound system. Specific clinical applications and exam types include: โ€ข Fetal/Obstetrics โ€ข Abdominal (LOGIQ P9) โ€ข Pediatric โ€ข Small Organ (LOGIQ P9) โ€ข Neonatal Cephalic โ€ข Adult Cephalic โ€ข Cardiac (LOGIQ P9) โ€ข Peripheral Vascular โ€ข Musculo-skeletal Conventional and Superficial โ€ข Urology (LOGIQ P9) โ€ข Transrectal โ€ข Transvaginal โ€ข Intraoperative (LOGIQ P9) โ€ข Transesophageal

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