gudid Primary ID: A0623P911D

LEONE SPA (UDI A0623P911D)

Manufactured by LEONE SPA

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The LEONE SPA (Model/Catalog Number: A0623P911D) is a medical device manufactured by LEONE SPA. This product is indexed under FDA Product Code / Category Classification DYJ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: A0623P911D
Product Code / EMDN: DYJ
Device Name: EXPANDER CAD-CAM PARTNERS DESIGN 11mm
Database Sync Date: 2026-08-09 09:04:34

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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Frequently Asked Questions

Who is the primary manufacturer of LEONE SPA?

The registered manufacturer of record for LEONE SPA is LEONE SPA.

What is the Primary UDI-DI identifier for LEONE SPA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A0623P911D.

What classification code is assigned to this device?

This device is registered under product classification code DYJ.

Similar Classification Devices (DYJ)

Other Devices by LEONE SPA

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