gudid Primary ID: VI001

Cavex Vibringe (UDI VI001)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Cavex Vibringe (Model/Catalog Number: VI001) is a medical device manufactured by Cavex Holland B.V.. This product is indexed under FDA Product Code / Category Classification EIC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: VI001
Product Code / EMDN: EIC
Device Name: Edodontic Irrigating Device
Database Sync Date: 2026-08-09 09:07:32

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Cavex Vibringe?

The registered manufacturer of record for Cavex Vibringe is Cavex Holland B.V..

What is the Primary UDI-DI identifier for Cavex Vibringe?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VI001.

What classification code is assigned to this device?

This device is registered under product classification code EIC.

Similar Classification Devices (EIC)

Other Devices by Cavex Holland B.V.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint