gudid
Primary ID: 3001-01-1-902
AMTRION Infusion S-0725-F-2-S (UDI 3001-01-1-902)
Manufactured by Amtrion GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AMTRION Infusion S-0725-F-2-S - Primary ID 3001-01-1-902
Device Regulatory Overview
The AMTRION Infusion S-0725-F-2-S (Model/Catalog Number: 3001-01-1-902) is a medical device manufactured by Amtrion GmbH. This product is indexed under FDA Product Code / Category Classification FOX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3001-01-1-902
- Product Code / EMDN
- FOX
- Device Name
- Database Sync Date
- 2026-08-09 09:17:35
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 AMTRION Infusion S-0725-F-2-S?
The registered manufacturer of record for AMTRION Infusion S-0725-F-2-S is Amtrion GmbH.
What is the Primary UDI-DI identifier for AMTRION Infusion S-0725-F-2-S?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3001-01-1-902.
What classification code is assigned to this device?
This device is registered under product classification code FOX.
Similar Classification Devices (FOX)
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