eudamed_udi
Primary ID: 00842318195838
Genesis AI 24 IIC NW (UDI 00842318195838)
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 24 IIC NW - Primary ID 00842318195838
Device Regulatory Overview
The Genesis AI 24 IIC NW (Model/Catalog Number: 72021-SHT) is a medical device manufactured by Starkey Laboratories Inc.. This product is indexed under FDA Product Code / Category Classification Y2145060204 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 72021-SHT
- Product Code / EMDN
- Y2145060204
- Device Name
- Genesis AI Custom
- Database Sync Date
- 2026-08-09 16:28:59
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 24 IIC NW?
The registered manufacturer of record for Genesis AI 24 IIC NW is Starkey Laboratories Inc..
What is the Primary UDI-DI identifier for Genesis AI 24 IIC NW?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00842318195838.
What classification code is assigned to this device?
This device is registered under product classification code Y2145060204.
Similar Classification Devices (Y2145060204)
Other Devices by Starkey Laboratories Inc.
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