GUDIDData
eudamed_udi Primary ID: 05056091022440

Ixion Posterior Band Remover (Short) (UDI 05056091022440)

Manufactured by DB Orthodontics Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ixion Posterior Band Remover (Short) - Primary ID 05056091022440

Device Regulatory Overview

The Ixion Posterior Band Remover (Short) (Model/Catalog Number: IX825) 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
IX825
Product Code / EMDN
L150702
Device Name
Ixion Instruments - Orthodontic Pliers
Database Sync Date
2026-08-09 16:48:43

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Ixion Posterior Band Remover (Short)?

The registered manufacturer of record for Ixion Posterior Band Remover (Short) is DB Orthodontics Limited.

What is the Primary UDI-DI identifier for Ixion Posterior Band Remover (Short)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05056091022440.

What classification code is assigned to this device?

This device is registered under product classification code L150702.

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