eudamed_udi
Primary ID: 05056091023317
Ixion Soft Ligature Cutter (UDI 05056091023317)
Manufactured by DB Orthodontics Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ixion Soft Ligature Cutter - Primary ID 05056091023317
Device Regulatory Overview
The Ixion Soft Ligature Cutter (Model/Catalog Number: IXR913) is a medical device manufactured by DB Orthodontics Limited. This product is indexed under FDA Product Code / Category Classification L150703 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IXR913
- Product Code / EMDN
- L150703
- Device Name
- Ixion Instruments - Orthodontic Cutters
- Database Sync Date
- 2026-08-09 16:30:00
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 Soft Ligature Cutter?
The registered manufacturer of record for Ixion Soft Ligature Cutter is DB Orthodontics Limited.
What is the Primary UDI-DI identifier for Ixion Soft Ligature Cutter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05056091023317.
What classification code is assigned to this device?
This device is registered under product classification code L150703.
Similar Classification Devices (L150703)
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