gudid Primary ID: 1.5.8

SilentCloud Mobile App (UDI 1.5.8)

Manufactured by Sonova AG

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

Scannable UDI-DI Representation

Device Regulatory Overview

The SilentCloud Mobile App (Model/Catalog Number: 1.5.8) is a medical device manufactured by Sonova AG. This product is indexed under FDA Product Code / Category Classification KLW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1.5.8
Product Code / EMDN: KLW
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 SilentCloud Mobile App?

The registered manufacturer of record for SilentCloud Mobile App is Sonova AG.

What is the Primary UDI-DI identifier for SilentCloud Mobile App?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.5.8.

What classification code is assigned to this device?

This device is registered under product classification code KLW.

Similar Classification Devices (KLW)

Other Devices by Sonova AG

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