gudid Primary ID: uDR 596i

uDR (UDI uDR 596i)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The uDR (Model/Catalog Number: uDR 596i) is a medical device manufactured by UIH TECHNOLOGIES LLC. This product is indexed under FDA Product Code / Category Classification MQB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: uDR 596i
Product Code / EMDN: MQB
Device Name: The uDR 596i Radiographic system is intended to be used by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, limbs and trunk. Not for mammography.
Database Sync Date: 2026-08-09 09:06:43

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 uDR?

The registered manufacturer of record for uDR is UIH TECHNOLOGIES LLC.

What is the Primary UDI-DI identifier for uDR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is uDR 596i.

What classification code is assigned to this device?

This device is registered under product classification code MQB.

Similar Classification Devices (MQB)

Other Devices by UIH TECHNOLOGIES LLC

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