N/A (UDI U90B Pro)

Manufactured by Shenzhen Urion Technology Co., Ltd

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The N/A (Model/Catalog Number: U90B Pro) is a medical device manufactured by Shenzhen Urion Technology Co., Ltd. This product is indexed under FDA Product Code / Category Classification DXN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: U90B Pro
Product Code / EMDN: DXN
Device Name
Database Sync Date: 2026-08-09 09:05:25

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 N/A?

The registered manufacturer of record for N/A is Shenzhen Urion Technology Co., Ltd.

What is the Primary UDI-DI identifier for N/A?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is U90B Pro.

What classification code is assigned to this device?

This device is registered under product classification code DXN.

Similar Classification Devices (DXN)

Other Devices by Shenzhen Urion Technology Co., Ltd

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