GUDIDData
gudid Primary ID: S2050

Solax (UDI S2050)

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 S2050

Device Regulatory Overview

The Solax (Model/Catalog Number: S2050) is a medical device manufactured by Guangdong Prestige Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification INI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
S2050
Product Code / EMDN
INI
Device Name
Electric Scooter
Database Sync Date
2026-08-09 09:06:45

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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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 S2050.

What classification code is assigned to this device?

This device is registered under product classification code INI.

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