eudamed_udi
Primary ID: 07613389392067
Roger NeckLoop (02) (US, champagne) (UDI 07613389392067)
Manufactured by Sonova AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Roger NeckLoop (02) (US, champagne) - Primary ID 07613389392067
Device Regulatory Overview
The Roger NeckLoop (02) (US, champagne) (Model/Catalog Number: 056-4004-P5211) is a medical device manufactured by Sonova AG. This product is indexed under FDA Product Code / Category Classification Y214580 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 056-4004-P5211
- Product Code / EMDN
- Y214580
- Device Name
- Wireless HA receivers
- Database Sync Date
- 2026-08-09 16:29:08
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 Roger NeckLoop (02) (US, champagne)?
The registered manufacturer of record for Roger NeckLoop (02) (US, champagne) is Sonova AG.
What is the Primary UDI-DI identifier for Roger NeckLoop (02) (US, champagne)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07613389392067.
What classification code is assigned to this device?
This device is registered under product classification code Y214580.
Similar Classification Devices (Y214580)
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