eudamed_udi
Primary ID: 05415168001113
Transferrin (UDI 05415168001113)
Manufactured by Diagam S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Transferrin - Primary ID 05415168001113
Device Regulatory Overview
The Transferrin (Model/Catalog Number: TFTUR-L00/AU) is a medical device manufactured by Diagam S.A.. This product is indexed under FDA Product Code / Category Classification W0102010307 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TFTUR-L00/AU
- Product Code / EMDN
- W0102010307
- Device Name
- Transferrin
- Database Sync Date
- 2026-08-09 16:30:18
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 Transferrin?
The registered manufacturer of record for Transferrin is Diagam S.A..
What is the Primary UDI-DI identifier for Transferrin?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05415168001113.
What classification code is assigned to this device?
This device is registered under product classification code W0102010307.
Similar Classification Devices (W0102010307)
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