eudamed_udi
Primary ID: 05204309175246
UREA (UDI 05204309175246)
Manufactured by Medicon Hellas SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for UREA - Primary ID 05204309175246
Device Regulatory Overview
The UREA (Model/Catalog Number: 1516-0020) is a medical device manufactured by Medicon Hellas SA. This product is indexed under FDA Product Code / Category Classification W01010204 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1516-0020
- Product Code / EMDN
- W01010204
- Device Name
- UREA
- Database Sync Date
- 2026-08-09 16:50:37
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 UREA?
The registered manufacturer of record for UREA is Medicon Hellas SA.
What is the Primary UDI-DI identifier for UREA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05204309175246.
What classification code is assigned to this device?
This device is registered under product classification code W01010204.
Similar Classification Devices (W01010204)
Other Devices by Medicon Hellas SA
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