GUDIDData
eudamed_udi Primary ID: 03666628002566

Gélose Mueller Hinton - Boite ronde 90 mm (UDI 03666628002566)

Manufactured by INTELLIGENCE ARTIFICIELLE APPLICATIONS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Gélose Mueller Hinton - Boite ronde 90 mm - Primary ID 03666628002566

Device Regulatory Overview

The Gélose Mueller Hinton - Boite ronde 90 mm (Model/Catalog Number: 020001) is a medical device manufactured by INTELLIGENCE ARTIFICIELLE APPLICATIONS. This product is indexed under FDA Product Code / Category Classification W0104010403 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
020001
Product Code / EMDN
W0104010403
Device Name
Milieu gélosé
Database Sync Date
2026-08-09 18:39:50

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Gélose Mueller Hinton - Boite ronde 90 mm?

The registered manufacturer of record for Gélose Mueller Hinton - Boite ronde 90 mm is INTELLIGENCE ARTIFICIELLE APPLICATIONS.

What is the Primary UDI-DI identifier for Gélose Mueller Hinton - Boite ronde 90 mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03666628002566.

What classification code is assigned to this device?

This device is registered under product classification code W0104010403.

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