Vigidental (UDI 05419980376626)

Manufactured by Vigident

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Vigidental (Model/Catalog Number: S1) is a medical device manufactured by Vigident. This product is indexed under FDA Product Code / Category Classification V92 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: S1
Product Code / EMDN: V92
Device Name: Vigidental
Database Sync Date: 2026-08-09 16:28:59

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 Vigidental?

The registered manufacturer of record for Vigidental is Vigident.

What is the Primary UDI-DI identifier for Vigidental?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05419980376626.

What classification code is assigned to this device?

This device is registered under product classification code V92.

Similar Classification Devices (V92)

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