GUDIDData
gudid Primary ID: 410-3010

E-A-RTONE (UDI 410-3010)

Manufactured by 3M COMPANY

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for E-A-RTONE - Primary ID 410-3010

Device Regulatory Overview

The E-A-RTONE (Model/Catalog Number: 410-3010) is a medical device manufactured by 3M COMPANY. This product is indexed under FDA Product Code / Category Classification EWO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
410-3010
Product Code / EMDN
EWO
Device Name
3M(TM) E-A-RTONE(TM) Insert Earphone 3A 10 ohm Original Equipment Manufacturer model 410-3010, 1/case
Database Sync Date
2026-08-09 09:08:45

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 E-A-RTONE?

The registered manufacturer of record for E-A-RTONE is 3M COMPANY.

What is the Primary UDI-DI identifier for E-A-RTONE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 410-3010.

What classification code is assigned to this device?

This device is registered under product classification code EWO.

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