eudamed_udi
Primary ID: 04056839062722
HA MOTION SA 3PX GR (UDI 04056839062722)
Manufactured by Signia GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HA MOTION SA 3PX GR - Primary ID 04056839062722
Device Regulatory Overview
The HA MOTION SA 3PX GR (Model/Catalog Number: 10934504) is a medical device manufactured by Signia GmbH. This product is indexed under FDA Product Code / Category Classification Y2145060101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10934504
- Product Code / EMDN
- Y2145060101
- Device Name
- BTE
- Database Sync Date
- 2026-08-09 16:30:10
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 SA 3PX GR?
The registered manufacturer of record for HA MOTION SA 3PX GR is Signia GmbH.
What is the Primary UDI-DI identifier for HA MOTION SA 3PX GR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04056839062722.
What classification code is assigned to this device?
This device is registered under product classification code Y2145060101.
Similar Classification Devices (Y2145060101)
Other Devices by Signia GmbH
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