GUDIDData
gudid Primary ID: VNG BASIC WIRELESS - XPR

VNG (UDI VNG BASIC WIRELESS - XPR)

Manufactured by INVENTIS SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VNG - Primary ID VNG BASIC WIRELESS - XPR

Device Regulatory Overview

The VNG (Model/Catalog Number: VNG BASIC WIRELESS - XPR) is a medical device manufactured by INVENTIS SRL. This product is indexed under FDA Product Code / Category Classification GWN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
VNG BASIC WIRELESS - XPR
Product Code / EMDN
GWN
Device Name
Video nystagmograph
Database Sync Date
2026-08-09 09:04:31

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?

The registered manufacturer of record for VNG is INVENTIS SRL.

What is the Primary UDI-DI identifier for VNG?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VNG BASIC WIRELESS - XPR.

What classification code is assigned to this device?

This device is registered under product classification code GWN.

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