eudamed_udi
Primary ID: 05714880273922
HA MOTION C&G SP 7IX PRL (UDI 05714880273922)
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 7IX PRL - Primary ID 05714880273922
Device Regulatory Overview
The HA MOTION C&G SP 7IX PRL (Model/Catalog Number: 21043104) 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
- 21043104
- Product Code / EMDN
- Y2145060101
- Device Name
- BTE
- Database Sync Date
- 2026-08-09 16:28:56
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of HA MOTION C&G SP 7IX PRL?
The registered manufacturer of record for HA MOTION C&G SP 7IX PRL is WSAUD A/S.
What is the Primary UDI-DI identifier for HA MOTION C&G SP 7IX PRL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05714880273922.
What classification code is assigned to this device?
This device is registered under product classification code Y2145060101.
Similar Classification Devices (Y2145060101)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint