gudid
Primary ID: S8 Exp
SonoScape (UDI S8 Exp)
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 S8 Exp
Device Regulatory Overview
The SonoScape (Model/Catalog Number: S8 Exp) 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
- S8 Exp
- Product Code / EMDN
- ITX
- Device Name
- S8 Exp Portable Digital Color Doppler Ultrasound System
- Database Sync Date
- 2026-08-09 09:05:30
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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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 S8 Exp.
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.
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