gudid
Primary ID: RT/USA
contact forte (UDI RT/USA)
Manufactured by BHM-Tech Produktionsgesellschaft m.b.H.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for contact forte - Primary ID RT/USA
Device Regulatory Overview
The contact forte (Model/Catalog Number: RT/USA) 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
- RT/USA
- Product Code / EMDN
- LXB
- Device Name
- bone conduction hearing aid, RT/red
- 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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of contact forte?
The registered manufacturer of record for contact forte is BHM-Tech Produktionsgesellschaft m.b.H..
What is the Primary UDI-DI identifier for contact forte?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RT/USA.
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.
Programmatic Export
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