eudamed_udi
Primary ID: 04260760131499
Potato dextrose agar (UDI 04260760131499)
Manufactured by Solabia Xebios GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Potato dextrose agar - Primary ID 04260760131499
Device Regulatory Overview
The Potato dextrose agar (Model/Catalog Number: 11.0201) 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
- 11.0201
- Product Code / EMDN
- W0104030201
- Device Name
- Potato dextrose agar
- Database Sync Date
- 2026-08-09 16:47:32
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 Potato dextrose agar?
The registered manufacturer of record for Potato dextrose agar is Solabia Xebios GmbH.
What is the Primary UDI-DI identifier for Potato dextrose agar?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260760131499.
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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