eudamed_udi
Primary ID: 08427734034026
DESFI-DORMO (UDI 08427734034026)
Manufactured by Telic, S.A.U.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DESFI-DORMO - Primary ID 08427734034026
Device Regulatory Overview
The DESFI-DORMO (Model/Catalog Number: EDC-2045) is a medical device manufactured by Telic, S.A.U.. This product is indexed under FDA Product Code / Category Classification C020480 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EDC-2045
- Product Code / EMDN
- C020480
- Device Name
- Electrodos de desfibrilación con cable para paciente adulto-pediátrico
- Database Sync Date
- 2026-08-09 16:28:51
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 DESFI-DORMO?
The registered manufacturer of record for DESFI-DORMO is Telic, S.A.U..
What is the Primary UDI-DI identifier for DESFI-DORMO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08427734034026.
What classification code is assigned to this device?
This device is registered under product classification code C020480.
Similar Classification Devices (C020480)
Other Devices by Telic, S.A.U.
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