gudid Primary ID: Synapsys VHIT Plus

Synapsys VHIT (UDI Synapsys VHIT Plus)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Synapsys VHIT (Model/Catalog Number: Synapsys VHIT Plus) 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: Synapsys VHIT Plus
Product Code / EMDN: GWN
Device Name: Video Head Impulse Test device
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 Synapsys VHIT?

The registered manufacturer of record for Synapsys VHIT is INVENTIS SRL.

What is the Primary UDI-DI identifier for Synapsys VHIT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Synapsys VHIT Plus.

What classification code is assigned to this device?

This device is registered under product classification code GWN.

Similar Classification Devices (GWN)

Other Devices by INVENTIS SRL

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