eudamed_udi
Primary ID: 04260760134438
GC Agar + Haemoglobine + vitox (UDI 04260760134438)
Manufactured by Solabia Xebios GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GC Agar + Haemoglobine + vitox - Primary ID 04260760134438
Device Regulatory Overview
The GC Agar + Haemoglobine + vitox (Model/Catalog Number: G092.02.0025) is a medical device manufactured by Solabia Xebios GmbH. This product is indexed under FDA Product Code / Category Classification W0104010405 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- G092.02.0025
- Product Code / EMDN
- W0104010405
- Device Name
- GC Agar + Haemoglobine + vitox
- Database Sync Date
- 2026-08-09 16:28:49
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 GC Agar + Haemoglobine + vitox?
The registered manufacturer of record for GC Agar + Haemoglobine + vitox is Solabia Xebios GmbH.
What is the Primary UDI-DI identifier for GC Agar + Haemoglobine + vitox?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260760134438.
What classification code is assigned to this device?
This device is registered under product classification code W0104010405.
Similar Classification Devices (W0104010405)
Other Devices by Solabia Xebios GmbH
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