VNG 3D (UDI RX1)

Manufactured by Ecleris

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

Scannable UDI-DI Representation

Device Regulatory Overview

The VNG 3D (Model/Catalog Number: RX1) is a medical device manufactured by Ecleris. This product is indexed under FDA Product Code / Category Classification GWN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: RX1
Product Code / EMDN: GWN
Device Name: VIDEONISTAGMOGRAPHY SYSTEM
Database Sync Date: 2026-08-09 09:18:01

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 VNG 3D?

The registered manufacturer of record for VNG 3D is Ecleris.

What is the Primary UDI-DI identifier for VNG 3D?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RX1.

What classification code is assigned to this device?

This device is registered under product classification code GWN.

Similar Classification Devices (GWN)

Other Devices by Ecleris

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