eudamed_udi
Primary ID: 05056091026110
Ixion Fine Tipped Weingart (UDI 05056091026110)
Manufactured by DB Orthodontics Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ixion Fine Tipped Weingart - Primary ID 05056091026110
Device Regulatory Overview
The Ixion Fine Tipped Weingart (Model/Catalog Number: IXR804) is a medical device manufactured by DB Orthodontics Limited. This product is indexed under FDA Product Code / Category Classification L03130499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IXR804
- Product Code / EMDN
- L03130499
- Device Name
- Ixion Instruments - Grasping Forceps
- Database Sync Date
- 2026-08-09 16:50:12
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 Fine Tipped Weingart?
The registered manufacturer of record for Ixion Fine Tipped Weingart is DB Orthodontics Limited.
What is the Primary UDI-DI identifier for Ixion Fine Tipped Weingart?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05056091026110.
What classification code is assigned to this device?
This device is registered under product classification code L03130499.
Similar Classification Devices (L03130499)
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