eudamed_udi
Primary ID: 00842318179333
LIVIO Edge AI HS R (UDI 00842318179333)
Manufactured by Starkey Laboratories Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LIVIO Edge AI HS R - Primary ID 00842318179333
Device Regulatory Overview
The LIVIO Edge AI HS R (Model/Catalog Number: 63208) is a medical device manufactured by Starkey Laboratories Inc.. This product is indexed under FDA Product Code / Category Classification Y2145060202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 63208
- Product Code / EMDN
- Y2145060202
- Device Name
- Starkey Livio Custom
- Database Sync Date
- 2026-08-09 16:48:33
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 LIVIO Edge AI HS R?
The registered manufacturer of record for LIVIO Edge AI HS R is Starkey Laboratories Inc..
What is the Primary UDI-DI identifier for LIVIO Edge AI HS R?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00842318179333.
What classification code is assigned to this device?
This device is registered under product classification code Y2145060202.
Similar Classification Devices (Y2145060202)
Other Devices by Starkey Laboratories Inc.
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