eudamed_udi
Primary ID: 04260760133448
Malt extract agar (UDI 04260760133448)
Manufactured by Solabia Xebios GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Malt extract agar - Primary ID 04260760133448
Device Regulatory Overview
The Malt extract agar (Model/Catalog Number: 11.1947) 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
- 11.1947
- Product Code / EMDN
- W0104030201
- Device Name
- Malt extract agar
- Database Sync Date
- 2026-08-09 18:52:35
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Malt extract agar?
The registered manufacturer of record for Malt extract agar is Solabia Xebios GmbH.
What is the Primary UDI-DI identifier for Malt extract agar?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260760133448.
What classification code is assigned to this device?
This device is registered under product classification code W0104030201.
Similar Classification Devices (W0104030201)
Other Devices by Solabia Xebios GmbH
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