gudid Primary ID: NuEar Noble AI 16 HS R

NUEAR (UDI NuEar Noble AI 16 HS R)

Manufactured by Starkey Laboratories, Inc.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The NUEAR (Model/Catalog Number: NuEar Noble AI 16 HS R) is a medical device manufactured by Starkey Laboratories, Inc.. This product is indexed under FDA Product Code / Category Classification KLW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: NuEar Noble AI 16 HS R
Product Code / EMDN: KLW
Device Name
Database Sync Date: 2026-08-09 09:07:49

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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Frequently Asked Questions

Who is the primary manufacturer of NUEAR?

The registered manufacturer of record for NUEAR is Starkey Laboratories, Inc..

What is the Primary UDI-DI identifier for NUEAR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is NuEar Noble AI 16 HS R.

What classification code is assigned to this device?

This device is registered under product classification code KLW.

Similar Classification Devices (KLW)

Other Devices by Starkey Laboratories, Inc.

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