Diagnostic Ultrasound System
- UID
- IMP/MD/2023/000729_6c713851603c6184fa7947aa97f4294f_57031f92dcac59dbe51434714ade070c
- Device class
- Class C
- Brand name
- ARIETTA
- License holder
- Pentax Medical India Private Limited
- Approving authority
- CDSCO
- Product information
- This system is intended for use by qualified persons for performing tomographic and hemodynamic diagnoses of the following parts of the human body: • Thorax • Abdomen • Perineal and pelvic internal organs • Lower limbs • Back • Upper limbs • Head • Neck Do not use this system for any purpose other than those stated above
Diagnostic Ultrasound System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000729_6c713851603c6184fa7947aa97f4294f_57031f92dcac59dbe51434714ade070c. This device is marketed under the brand name ARIETTA. The license holder is Pentax Medical India 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.