gudid
Primary ID: audifon APP 1.4.2
audifon (UDI audifon APP 1.4.2)
Manufactured by audifon GmbH & Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for audifon - Primary ID audifon APP 1.4.2
Device Regulatory Overview
The audifon (Model/Catalog Number: audifon APP 1.4.2) is a medical device manufactured by audifon GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification ETW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- audifon APP 1.4.2
- Product Code / EMDN
- ETW
- Device Name
- audifon APP
- Database Sync Date
- 2026-08-09 09:23:55
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 audifon?
The registered manufacturer of record for audifon is audifon GmbH & Co. KG.
What is the Primary UDI-DI identifier for audifon?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is audifon APP 1.4.2.
What classification code is assigned to this device?
This device is registered under product classification code ETW.
Similar Classification Devices (ETW)
Other Devices by audifon GmbH & Co. KG
Programmatic Export
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