eudamed_udi
Primary ID: 03663996018724
COMEPA (UDI 03663996018724)
Manufactured by Telic, S.A.U.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for COMEPA - Primary ID 03663996018724
Device Regulatory Overview
The COMEPA (Model/Catalog Number: 3G250EC) is a medical device manufactured by Telic, S.A.U.. This product is indexed under FDA Product Code / Category Classification C020599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3G250EC
- Product Code / EMDN
- C020599
- Device Name
- Electro-gel
- Database Sync Date
- 2026-08-09 16:30:07
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 COMEPA?
The registered manufacturer of record for COMEPA is Telic, S.A.U..
What is the Primary UDI-DI identifier for COMEPA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03663996018724.
What classification code is assigned to this device?
This device is registered under product classification code C020599.
Similar Classification Devices (C020599)
Other Devices by Telic, S.A.U.
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