GUDIDData
eudamed_udi Primary ID: 00840388204559

NuEar Edge AI 24 CIC (UDI 00840388204559)

Manufactured by Starkey Laboratories Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NuEar Edge AI 24 CIC - Primary ID 00840388204559

Device Regulatory Overview

The NuEar Edge AI 24 CIC (Model/Catalog Number: 72096-NUE) is a medical device manufactured by Starkey Laboratories Inc.. This product is indexed under FDA Product Code / Category Classification Y2145060203 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
72096-NUE
Product Code / EMDN
Y2145060203
Device Name
Edge AI Custom
Database Sync Date
2026-08-09 16:29:38

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of NuEar Edge AI 24 CIC?

The registered manufacturer of record for NuEar Edge AI 24 CIC is Starkey Laboratories Inc..

What is the Primary UDI-DI identifier for NuEar Edge AI 24 CIC?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840388204559.

What classification code is assigned to this device?

This device is registered under product classification code Y2145060203.

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