SIUI (UDI SR-2300)
Manufactured by Shantou Institute of Ultrasonic Instruments Co., Ltd.
Device Regulatory Overview
The SIUI (Model/Catalog Number: SR-2300) is a medical device manufactured by Shantou Institute of Ultrasonic Instruments Co., Ltd.. This product is indexed under FDA Product Code / Category Classification IZL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SR-2300
- Product Code / EMDN
- IZL
- Device Name
- Portable DR Imaging System
- Database Sync Date
- 2026-08-09 09:04:56
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 SIUI?
The registered manufacturer of record for SIUI is Shantou Institute of Ultrasonic Instruments Co., Ltd..
What is the Primary UDI-DI identifier for SIUI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SR-2300.
What classification code is assigned to this device?
This device is registered under product classification code IZL.
Similar Classification Devices (IZL)
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