GUDIDData
gudid Primary ID: VIDEOSTAR II

Instrumentation Difra (UDI VIDEOSTAR II)

Manufactured by Instrumentation Difra SA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Instrumentation Difra - Primary ID VIDEOSTAR II

Device Regulatory Overview

The Instrumentation Difra (Model/Catalog Number: VIDEOSTAR II) is a medical device manufactured by Instrumentation Difra SA. This product is indexed under FDA Product Code / Category Classification GWN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
VIDEOSTAR II
Product Code / EMDN
GWN
Device Name
The VIDEOSTAR is a digital videoscopy system. It is designed to allow qualified personnel to visualize eye reaction of the patient and record digital video.Freefield videonystagmoscope digital USB2
Database Sync Date
2026-08-09 09:34:46

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Instrumentation Difra?

The registered manufacturer of record for Instrumentation Difra is Instrumentation Difra SA.

What is the Primary UDI-DI identifier for Instrumentation Difra?

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

What classification code is assigned to this device?

This device is registered under product classification code GWN.

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