eudamed_udi
Primary ID: 05204309120963
ACE (UDI 05204309120963)
Manufactured by Medicon Hellas SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ACE - Primary ID 05204309120963
Device Regulatory Overview
The ACE (Model/Catalog Number: 1419-1162) is a medical device manufactured by Medicon Hellas SA. This product is indexed under FDA Product Code / Category Classification W01010109 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1419-1162
- Product Code / EMDN
- W01010109
- Device Name
- ACE
- Database Sync Date
- 2026-08-09 17:29:40
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 ACE?
The registered manufacturer of record for ACE is Medicon Hellas SA.
What is the Primary UDI-DI identifier for ACE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05204309120963.
What classification code is assigned to this device?
This device is registered under product classification code W01010109.
Similar Classification Devices (W01010109)
Other Devices by Medicon Hellas SA
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