NuEar NE Series AI 10 RIC R (UDI 00840388209837)
Manufactured by Starkey Laboratories Inc.
Device Regulatory Overview
The NuEar NE Series AI 10 RIC R (Model/Catalog Number: 63402-4) 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
- 63402-4
- Product Code / EMDN
- Y2145060102
- Device Name
- G Series AI
- Database Sync Date
- 2026-08-09 16:48:36
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 NuEar NE Series AI 10 RIC R?
The registered manufacturer of record for NuEar NE Series AI 10 RIC R is Starkey Laboratories Inc..
What is the Primary UDI-DI identifier for NuEar NE Series AI 10 RIC R?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840388209837.
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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