eudamed_udi
Primary ID: 07613389828535
Argosy V9-M (pewter) (UDI 07613389828535)
Manufactured by Sonova AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Argosy V9-M (pewter) - Primary ID 07613389828535
Device Regulatory Overview
The Argosy V9-M (pewter) (Model/Catalog Number: 050-6864-P745) 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
- 050-6864-P745
- Product Code / EMDN
- Y2145060101
- Device Name
- Sonova BTE hearing aids
- Database Sync Date
- 2026-08-09 16:28:55
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 Argosy V9-M (pewter)?
The registered manufacturer of record for Argosy V9-M (pewter) is Sonova AG.
What is the Primary UDI-DI identifier for Argosy V9-M (pewter)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07613389828535.
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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