GUDIDData
eudamed_udi Primary ID: 03760035442028

STABIDOIGT ALU MOUSSE (UDI 03760035442028)

Manufactured by GROUPE SOBER SAS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STABIDOIGT ALU MOUSSE - Primary ID 03760035442028

Device Regulatory Overview

The STABIDOIGT ALU MOUSSE (Model/Catalog Number: STABIDOIGT ALU MOUSSE) is a medical device manufactured by GROUPE SOBER SAS. This product is indexed under FDA Product Code / Category Classification Y060603 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
STABIDOIGT ALU MOUSSE
Product Code / EMDN
Y060603
Device Name
STABIDOIGT ALU MOUSSE
Database Sync Date
2026-08-09 16:29:39

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 STABIDOIGT ALU MOUSSE?

The registered manufacturer of record for STABIDOIGT ALU MOUSSE is GROUPE SOBER SAS.

What is the Primary UDI-DI identifier for STABIDOIGT ALU MOUSSE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760035442028.

What classification code is assigned to this device?

This device is registered under product classification code Y060603.

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