eudamed_udi
Primary ID: 06970990830304
Solax (UDI 06970990830304)
Manufactured by Guangdong Prestige Technology Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Solax - Primary ID 06970990830304
Device Regulatory Overview
The Solax (Model/Catalog Number: S3023) is a medical device manufactured by Guangdong Prestige Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Y122124 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S3023
- Product Code / EMDN
- Y122124
- Device Name
- Electric Scooter
- Database Sync Date
- 2026-08-09 16:30:19
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 Solax?
The registered manufacturer of record for Solax is Guangdong Prestige Technology Co., Ltd..
What is the Primary UDI-DI identifier for Solax?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970990830304.
What classification code is assigned to this device?
This device is registered under product classification code Y122124.
Similar Classification Devices (Y122124)
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