eudamed_udi
Primary ID: 05415168002806
Ceruloplasmin (UDI 05415168002806)
Manufactured by Diagam S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ceruloplasmin - Primary ID 05415168002806
Device Regulatory Overview
The Ceruloplasmin (Model/Catalog Number: CETUR-H00/COB) is a medical device manufactured by Diagam S.A.. This product is indexed under FDA Product Code / Category Classification W0102010301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CETUR-H00/COB
- Product Code / EMDN
- W0102010301
- Device Name
- Ceruloplasmin
- Database Sync Date
- 2026-08-09 16:29:56
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 Ceruloplasmin?
The registered manufacturer of record for Ceruloplasmin is Diagam S.A..
What is the Primary UDI-DI identifier for Ceruloplasmin?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05415168002806.
What classification code is assigned to this device?
This device is registered under product classification code W0102010301.
Similar Classification Devices (W0102010301)
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