eudamed_udi Primary ID: 01220000532489

Actimove AluFoam Aluminum Finger Splint (UDI 01220000532489)

Manufactured by Span Link International, LLC

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Actimove AluFoam Aluminum Finger Splint (Model/Catalog Number: 72956-00004-00) is a medical device manufactured by Span Link International, LLC. This product is indexed under FDA Product Code / Category Classification Y060603 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 72956-00004-00
Product Code / EMDN: Y060603
Device Name: Actimove AluFoam Aluminum Finger Splint
Database Sync Date: 2026-08-09 16:28:52

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 Actimove AluFoam Aluminum Finger Splint?

The registered manufacturer of record for Actimove AluFoam Aluminum Finger Splint is Span Link International, LLC.

What is the Primary UDI-DI identifier for Actimove AluFoam Aluminum Finger Splint?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 01220000532489.

What classification code is assigned to this device?

This device is registered under product classification code Y060603.

Similar Classification Devices (Y060603)

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