eudamed_udi
Primary ID: D-030240-9811-311-1720AQ
KINDwings 1400 (UDI D-030240-9811-311-1720AQ)
Manufactured by audifon GmbH & Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KINDwings 1400 - Primary ID D-030240-9811-311-1720AQ
Device Regulatory Overview
The KINDwings 1400 (Model/Catalog Number: 030240-9811-311-1720) is a medical device manufactured by audifon GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification Y2145060102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 030240-9811-311-1720
- Product Code / EMDN
- Y2145060102
- Device Name
- Hearing aid
- Database Sync Date
- 2026-08-09 16:44:58
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 KINDwings 1400?
The registered manufacturer of record for KINDwings 1400 is audifon GmbH & Co. KG.
What is the Primary UDI-DI identifier for KINDwings 1400?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-030240-9811-311-1720AQ.
What classification code is assigned to this device?
This device is registered under product classification code Y2145060102.
Similar Classification Devices (Y2145060102)
Other Devices by audifon GmbH & Co. KG
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