GUDIDData
eudamed_udi Primary ID: 04260760130126

Sabouraud dextrose agar + aztreonam/vancomycin (UDI 04260760130126)

Manufactured by Solabia Xebios GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sabouraud dextrose agar + aztreonam/vancomycin - Primary ID 04260760130126

Device Regulatory Overview

The Sabouraud dextrose agar + aztreonam/vancomycin (Model/Catalog Number: 11.0448) is a medical device manufactured by Solabia Xebios GmbH. This product is indexed under FDA Product Code / Category Classification W0104030201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
11.0448
Product Code / EMDN
W0104030201
Device Name
Sabouraud dextrose agar + aztreonam/vancomycin
Database Sync Date
2026-08-09 17:18:58

Full Regulatory Attributes

πŸ”’ 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 Sabouraud dextrose agar + aztreonam/vancomycin?

The registered manufacturer of record for Sabouraud dextrose agar + aztreonam/vancomycin is Solabia Xebios GmbH.

What is the Primary UDI-DI identifier for Sabouraud dextrose agar + aztreonam/vancomycin?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260760130126.

What classification code is assigned to this device?

This device is registered under product classification code W0104030201.

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