gudid
Primary ID: S9 Pro
SonoScape (UDI S9 Pro)
Manufactured by SONOSCAPE MEDICAL CORP.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SonoScape - Primary ID S9 Pro
Device Regulatory Overview
The SonoScape (Model/Catalog Number: S9 Pro) is a medical device manufactured by SONOSCAPE MEDICAL CORP.. This product is indexed under FDA Product Code / Category Classification ITX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S9 Pro
- Product Code / EMDN
- ITX
- Device Name
- S9 Pro Portable Digital Color Doppler Ultrasound System
- Database Sync Date
- 2026-08-09 09:05:30
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of SonoScape?
The registered manufacturer of record for SonoScape is SONOSCAPE MEDICAL CORP..
What is the Primary UDI-DI identifier for SonoScape?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S9 Pro.
What classification code is assigned to this device?
This device is registered under product classification code ITX.
Similar Classification Devices (ITX)
Other Devices by SONOSCAPE MEDICAL CORP.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint