eudamed_udi Primary ID: 03615800014781

ANGELO 200 M BLEU PASTEL (UDI 03615800014781)

Manufactured by VILGO

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ANGELO 200 M BLEU PASTEL (Model/Catalog Number: 1060042S14) is a medical device manufactured by VILGO. This product is indexed under FDA Product Code / Category Classification Y120606 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1060042S14
Product Code / EMDN: Y120606
Device Name: ANGELO 200 M
Database Sync Date: 2026-08-09 16:29:16

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 ANGELO 200 M BLEU PASTEL?

The registered manufacturer of record for ANGELO 200 M BLEU PASTEL is VILGO.

What is the Primary UDI-DI identifier for ANGELO 200 M BLEU PASTEL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03615800014781.

What classification code is assigned to this device?

This device is registered under product classification code Y120606.

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