audifon (UDI eox S)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The audifon (Model/Catalog Number: eox S) is a medical device manufactured by audifon GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification OSM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: eox S
Product Code / EMDN: OSM
Device Name: BTE
Database Sync Date: 2026-08-09 09:23:55

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 audifon?

The registered manufacturer of record for audifon is audifon GmbH & Co. KG.

What is the Primary UDI-DI identifier for audifon?

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

What classification code is assigned to this device?

This device is registered under product classification code OSM.

Similar Classification Devices (OSM)

Other Devices by audifon GmbH & Co. KG

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