eudamed_udi
Primary ID: 04251737900422
StorAX Cary Blair (UDI 04251737900422)
Manufactured by Axon Biotech GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for StorAX Cary Blair - Primary ID 04251737900422
Device Regulatory Overview
The StorAX Cary Blair (Model/Catalog Number: AL0302_250) is a medical device manufactured by Axon Biotech GmbH. This product is indexed under FDA Product Code / Category Classification W05020199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AL0302_250
- Product Code / EMDN
- W05020199
- Device Name
- Transportgefäss Stuhlprobe
- Database Sync Date
- 2026-08-09 16:30:28
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 StorAX Cary Blair?
The registered manufacturer of record for StorAX Cary Blair is Axon Biotech GmbH.
What is the Primary UDI-DI identifier for StorAX Cary Blair?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251737900422.
What classification code is assigned to this device?
This device is registered under product classification code W05020199.
Similar Classification Devices (W05020199)
Other Devices by Axon Biotech GmbH
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