eudamed_udi Primary ID: 03615800045860

QUIEGO 3000 V2 (BRONZE/TERRE) (UDI 03615800045860)

Manufactured by VILGO

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

Scannable UDI-DI Representation

Device Regulatory Overview

The QUIEGO 3000 V2 (BRONZE/TERRE) (Model/Catalog Number: 2070092S08) is a medical device manufactured by VILGO. This product is indexed under FDA Product Code / Category Classification V080202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2070092S08
Product Code / EMDN: V080202
Device Name: QUIEGO 3000
Database Sync Date: 2026-08-09 16:28:45

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 QUIEGO 3000 V2 (BRONZE/TERRE)?

The registered manufacturer of record for QUIEGO 3000 V2 (BRONZE/TERRE) is VILGO.

What is the Primary UDI-DI identifier for QUIEGO 3000 V2 (BRONZE/TERRE)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03615800045860.

What classification code is assigned to this device?

This device is registered under product classification code V080202.

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