eudamed_udi
Primary ID: 00840388200117
Genesis AI 20 RIC 312 (UDI 00840388200117)
Manufactured by Starkey Laboratories Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Genesis AI 20 RIC 312 - Primary ID 00840388200117
Device Regulatory Overview
The Genesis AI 20 RIC 312 (Model/Catalog Number: 63344-1) 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
- 63344-1
- Product Code / EMDN
- Y2145060102
- Device Name
- Genesis AI Standard
- Database Sync Date
- 2026-08-09 16:48:22
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 Genesis AI 20 RIC 312?
The registered manufacturer of record for Genesis AI 20 RIC 312 is Starkey Laboratories Inc..
What is the Primary UDI-DI identifier for Genesis AI 20 RIC 312?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840388200117.
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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