eudamed_udi
Primary ID: 05204309137275
C3 (UDI 05204309137275)
Manufactured by Medicon Hellas SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for C3 - Primary ID 05204309137275
Device Regulatory Overview
The C3 (Model/Catalog Number: 1417-0760) is a medical device manufactured by Medicon Hellas SA. This product is indexed under FDA Product Code / Category Classification W0102010203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1417-0760
- Product Code / EMDN
- W0102010203
- Device Name
- C3
- Database Sync Date
- 2026-08-09 16:49:00
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 C3?
The registered manufacturer of record for C3 is Medicon Hellas SA.
What is the Primary UDI-DI identifier for C3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05204309137275.
What classification code is assigned to this device?
This device is registered under product classification code W0102010203.
Similar Classification Devices (W0102010203)
Other Devices by Medicon Hellas SA
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