GUDIDData
eudamed_udi Primary ID: 05715763006668

Footshell Forever R24 Black - I.D. 210mm (UDI 05715763006668)

Manufactured by Levitate Technology ApS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Footshell Forever R24 Black - I.D. 210mm - Primary ID 05715763006668

Device Regulatory Overview

The Footshell Forever R24 Black - I.D. 210mm (Model/Catalog Number: LTA110006) is a medical device manufactured by Levitate Technology ApS. This product is indexed under FDA Product Code / Category Classification Y062499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
LTA110006
Product Code / EMDN
Y062499
Device Name
Artificial Limb Components
Database Sync Date
2026-08-09 16:48:59

Full Regulatory Attributes

๐Ÿ”’ 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 Footshell Forever R24 Black - I.D. 210mm?

The registered manufacturer of record for Footshell Forever R24 Black - I.D. 210mm is Levitate Technology ApS.

What is the Primary UDI-DI identifier for Footshell Forever R24 Black - I.D. 210mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05715763006668.

What classification code is assigned to this device?

This device is registered under product classification code Y062499.

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