eudamed_udi
Primary ID: 07613389655261
AQ beat FS 9-R (mocha brown) (UDI 07613389655261)
Manufactured by Sonova AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AQ beat FS 9-R (mocha brown) - Primary ID 07613389655261
Device Regulatory Overview
The AQ beat FS 9-R (mocha brown) (Model/Catalog Number: 050-6848-UB) is a medical device manufactured by Sonova AG. This product is indexed under FDA Product Code / Category Classification Y2145060101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 050-6848-UB
- Product Code / EMDN
- Y2145060101
- Device Name
- Sonova BTE hearing aids
- Database Sync Date
- 2026-08-09 16:28:57
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 AQ beat FS 9-R (mocha brown)?
The registered manufacturer of record for AQ beat FS 9-R (mocha brown) is Sonova AG.
What is the Primary UDI-DI identifier for AQ beat FS 9-R (mocha brown)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07613389655261.
What classification code is assigned to this device?
This device is registered under product classification code Y2145060101.
Similar Classification Devices (Y2145060101)
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