eudamed_udi Primary ID: 03615800015757

GR 101 (NOIR/BORDEAUX) (UDI 03615800015757)

Manufactured by VILGO

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

Scannable UDI-DI Representation

Device Regulatory Overview

The GR 101 (NOIR/BORDEAUX) (Model/Catalog Number: 2010007S6) is a medical device manufactured by VILGO. This product is indexed under FDA Product Code / Category Classification Y091203 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2010007S6
Product Code / EMDN: Y091203
Device Name: GR 101
Database Sync Date: 2026-08-09 16:28:47

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 GR 101 (NOIR/BORDEAUX)?

The registered manufacturer of record for GR 101 (NOIR/BORDEAUX) is VILGO.

What is the Primary UDI-DI identifier for GR 101 (NOIR/BORDEAUX)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03615800015757.

What classification code is assigned to this device?

This device is registered under product classification code Y091203.

Similar Classification Devices (Y091203)

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