gudid
Primary ID: 395 400 025
Electrode (UDI 395 400 025)
Manufactured by SOPRO-COMEG GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Electrode - Primary ID 395 400 025
Device Regulatory Overview
The Electrode (Model/Catalog Number: 395 400 025) is a medical device manufactured by SOPRO-COMEG GmbH. This product is indexed under FDA Product Code / Category Classification FAS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 395 400 025
- Product Code / EMDN
- FAS
- Device Name
- Database Sync Date
- 2026-08-09 09:11:48
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 Electrode?
The registered manufacturer of record for Electrode is SOPRO-COMEG GmbH.
What is the Primary UDI-DI identifier for Electrode?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 395 400 025.
What classification code is assigned to this device?
This device is registered under product classification code FAS.
Similar Classification Devices (FAS)
Other Devices by SOPRO-COMEG GmbH
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