gudid
Primary ID: E-Board S
Immedia (UDI E-Board S)
Manufactured by Etac Immedia A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Immedia - Primary ID E-Board S
Device Regulatory Overview
The Immedia (Model/Catalog Number: E-Board S) is a medical device manufactured by Etac Immedia A/S. This product is indexed under FDA Product Code / Category Classification IKX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- E-Board S
- Product Code / EMDN
- IKX
- Device Name
- Database Sync Date
- 2026-08-09 09:33:31
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 Immedia?
The registered manufacturer of record for Immedia is Etac Immedia A/S.
What is the Primary UDI-DI identifier for Immedia?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E-Board S.
What classification code is assigned to this device?
This device is registered under product classification code IKX.
Similar Classification Devices (IKX)
Other Devices by Etac Immedia A/S
Programmatic Export
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