eudamed_udi
Primary ID: 05714464046560
Bernafon (UDI 05714464046560)
Manufactured by SBO Hearing A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bernafon - Primary ID 05714464046560
Device Regulatory Overview
The Bernafon (Model/Catalog Number: 236003) is a medical device manufactured by SBO Hearing A/S. This product is indexed under FDA Product Code / Category Classification Y2145060101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 236003
- Product Code / EMDN
- Y2145060101
- Device Name
- HI (BTE)
- Database Sync Date
- 2026-08-09 16:28:49
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 Bernafon?
The registered manufacturer of record for Bernafon is SBO Hearing A/S.
What is the Primary UDI-DI identifier for Bernafon?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05714464046560.
What classification code is assigned to this device?
This device is registered under product classification code Y2145060101.
Similar Classification Devices (Y2145060101)
Other Devices by SBO Hearing A/S
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