eudamed_udi Primary ID: 03615800008575

571 LAGON (UDI 03615800008575)

Manufactured by VILGO

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

Scannable UDI-DI Representation

Device Regulatory Overview

The 571 LAGON (Model/Catalog Number: 1020013S8) is a medical device manufactured by VILGO. This product is indexed under FDA Product Code / Category Classification Y12030601 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1020013S8
Product Code / EMDN: Y12030601
Device Name: 571
Database Sync Date: 2026-08-09 16:29:49

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 571 LAGON?

The registered manufacturer of record for 571 LAGON is VILGO.

What is the Primary UDI-DI identifier for 571 LAGON?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03615800008575.

What classification code is assigned to this device?

This device is registered under product classification code Y12030601.

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