eudamed_udi
Primary ID: 05714464000050
Philips (UDI 05714464000050)
Manufactured by SBO Hearing A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Philips - Primary ID 05714464000050
Device Regulatory Overview
The Philips (Model/Catalog Number: 194653) is a medical device manufactured by SBO Hearing A/S. This product is indexed under FDA Product Code / Category Classification Y214580 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 194653
- Product Code / EMDN
- Y214580
- Device Name
- TV Adapter
- Database Sync Date
- 2026-08-09 16:30:09
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 Philips?
The registered manufacturer of record for Philips is SBO Hearing A/S.
What is the Primary UDI-DI identifier for Philips?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05714464000050.
What classification code is assigned to this device?
This device is registered under product classification code Y214580.
Similar Classification Devices (Y214580)
Other Devices by SBO Hearing A/S
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