MedRx (UDI MedRx Kiosk)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The MedRx (Model/Catalog Number: MedRx Kiosk) is a medical device manufactured by MEDRX, INC.. This product is indexed under FDA Product Code / Category Classification EWO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MedRx Kiosk
Product Code / EMDN: EWO
Device Name
Database Sync Date: 2026-08-09 09:10:03

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 MedRx?

The registered manufacturer of record for MedRx is MEDRX, INC..

What is the Primary UDI-DI identifier for MedRx?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MedRx Kiosk.

What classification code is assigned to this device?

This device is registered under product classification code EWO.

Similar Classification Devices (EWO)

Other Devices by MEDRX, INC.

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