gudid Primary ID: contact forte/SW

Hearbow (UDI contact forte/SW)

Manufactured by BHM-Tech Produktionsgesellschaft m.b.H.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Hearbow (Model/Catalog Number: contact forte/SW) is a medical device manufactured by BHM-Tech Produktionsgesellschaft m.b.H.. This product is indexed under FDA Product Code / Category Classification LXB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: contact forte/SW
Product Code / EMDN: LXB
Device Name: Hearbow for contact forte, SW/blackAccessory for use with contact forte bone conduction hearing aid
Database Sync Date: 2026-08-09 09:29:33

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 Hearbow?

The registered manufacturer of record for Hearbow is BHM-Tech Produktionsgesellschaft m.b.H..

What is the Primary UDI-DI identifier for Hearbow?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is contact forte/SW.

What classification code is assigned to this device?

This device is registered under product classification code LXB.

Similar Classification Devices (LXB)

Other Devices by BHM-Tech Produktionsgesellschaft m.b.H.

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