gudid Primary ID: (sienna red)

Phonak Audo E30-Sphere (UDI (sienna red))

Manufactured by Sonova AG

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Phonak Audo E30-Sphere (Model/Catalog Number: (sienna red)) is a medical device manufactured by Sonova AG. This product is indexed under FDA Product Code / Category Classification OSM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: (sienna red)
Product Code / EMDN: OSM
Device Name
Database Sync Date: 2026-08-09 09:19:56

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 Phonak Audo E30-Sphere?

The registered manufacturer of record for Phonak Audo E30-Sphere is Sonova AG.

What is the Primary UDI-DI identifier for Phonak Audo E30-Sphere?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is (sienna red).

What classification code is assigned to this device?

This device is registered under product classification code OSM.

Similar Classification Devices (OSM)

Other Devices by Sonova AG

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