eudamed_udi
Primary ID: 00842318179340
LIVIO EDGE AI mRIC 312 (UDI 00842318179340)
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 mRIC 312 - Primary ID 00842318179340
Device Regulatory Overview
The LIVIO EDGE AI mRIC 312 (Model/Catalog Number: 63193) is a medical device manufactured by Starkey Laboratories Inc.. This product is indexed under FDA Product Code / Category Classification Y2145060102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 63193
- Product Code / EMDN
- Y2145060102
- Device Name
- Livio Standard RIC
- Database Sync Date
- 2026-08-09 16:47:15
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 mRIC 312?
The registered manufacturer of record for LIVIO EDGE AI mRIC 312 is Starkey Laboratories Inc..
What is the Primary UDI-DI identifier for LIVIO EDGE AI mRIC 312?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00842318179340.
What classification code is assigned to this device?
This device is registered under product classification code Y2145060102.
Similar Classification Devices (Y2145060102)
Other Devices by Starkey Laboratories Inc.
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