gudid
Primary ID: OneWayGlide Velour
Immedia (UDI OneWayGlide Velour)
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 OneWayGlide Velour
Device Regulatory Overview
The Immedia (Model/Catalog Number: OneWayGlide Velour) 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
- OneWayGlide Velour
- 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 OneWayGlide Velour.
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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