eudamed_udi
Primary ID: 05056091021948
Ixion Spring Former (UDI 05056091021948)
Manufactured by DB Orthodontics Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ixion Spring Former - Primary ID 05056091021948
Device Regulatory Overview
The Ixion Spring Former (Model/Catalog Number: IX165) is a medical device manufactured by DB Orthodontics Limited. This product is indexed under FDA Product Code / Category Classification L150702 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IX165
- Product Code / EMDN
- L150702
- Device Name
- Ixion Instruments - Orthodontic Pliers
- Database Sync Date
- 2026-08-09 16:45:48
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 Ixion Spring Former?
The registered manufacturer of record for Ixion Spring Former is DB Orthodontics Limited.
What is the Primary UDI-DI identifier for Ixion Spring Former?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05056091021948.
What classification code is assigned to this device?
This device is registered under product classification code L150702.
Similar Classification Devices (L150702)
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