eudamed_udi
Primary ID: 05714880274103
HA MOTION C&G SP 5IX DKC (UDI 05714880274103)
Manufactured by WSAUD A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HA MOTION C&G SP 5IX DKC - Primary ID 05714880274103
Device Regulatory Overview
The HA MOTION C&G SP 5IX DKC (Model/Catalog Number: 21043420) is a medical device manufactured by WSAUD A/S. This product is indexed under FDA Product Code / Category Classification Y2145060101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 21043420
- Product Code / EMDN
- Y2145060101
- Device Name
- BTE
- Database Sync Date
- 2026-08-09 16:28:58
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 HA MOTION C&G SP 5IX DKC?
The registered manufacturer of record for HA MOTION C&G SP 5IX DKC is WSAUD A/S.
What is the Primary UDI-DI identifier for HA MOTION C&G SP 5IX DKC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05714880274103.
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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