gudid Primary ID: (velvet black)

Phonak Terra BTE-UP (UDI (velvet black))

Manufactured by Sonova AG

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Phonak Terra BTE-UP (Model/Catalog Number: (velvet black)) 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: (velvet black)
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 Terra BTE-UP?

The registered manufacturer of record for Phonak Terra BTE-UP is Sonova AG.

What is the Primary UDI-DI identifier for Phonak Terra BTE-UP?

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

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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