eudamed_udi
Primary ID: 04251737901870
VTM 3ml (UDI 04251737901870)
Manufactured by Axon Biotech GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VTM 3ml - Primary ID 04251737901870
Device Regulatory Overview
The VTM 3ml (Model/Catalog Number: AL0632) is a medical device manufactured by Axon Biotech GmbH. This product is indexed under FDA Product Code / Category Classification W0104010203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AL0632
- Product Code / EMDN
- W0104010203
- Device Name
- Flüssige Medien
- Database Sync Date
- 2026-08-09 16:29:18
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 VTM 3ml?
The registered manufacturer of record for VTM 3ml is Axon Biotech GmbH.
What is the Primary UDI-DI identifier for VTM 3ml?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251737901870.
What classification code is assigned to this device?
This device is registered under product classification code W0104010203.
Similar Classification Devices (W0104010203)
Other Devices by Axon Biotech GmbH
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