eudamed_udi
Primary ID: 05415168010269
Rheumatoïd Factor (UDI 05415168010269)
Manufactured by Diagam S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rheumatoïd Factor - Primary ID 05415168010269
Device Regulatory Overview
The Rheumatoïd Factor (Model/Catalog Number: RFCOL-H00/ATE) is a medical device manufactured by Diagam S.A.. This product is indexed under FDA Product Code / Category Classification W01021110 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RFCOL-H00/ATE
- Product Code / EMDN
- W01021110
- Device Name
- Rheumatoïd Factor
- Database Sync Date
- 2026-08-09 16:50:14
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Rheumatoïd Factor?
The registered manufacturer of record for Rheumatoïd Factor is Diagam S.A..
What is the Primary UDI-DI identifier for Rheumatoïd Factor?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05415168010269.
What classification code is assigned to this device?
This device is registered under product classification code W01021110.
Similar Classification Devices (W01021110)
Other Devices by Diagam S.A.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint