GUDIDData
eudamed_udi Primary ID: 01230000153218

Actimove® Closed Shell Air Walker (UDI 01230000153218)

Manufactured by Span Link International, LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Actimove® Closed Shell Air Walker - Primary ID 01230000153218

Device Regulatory Overview

The Actimove® Closed Shell Air Walker (Model/Catalog Number: 76276-00031-01) is a medical device manufactured by Span Link International, LLC. This product is indexed under FDA Product Code / Category Classification Y06120601 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
76276-00031-01
Product Code / EMDN
Y06120601
Device Name
Actimove® Closed Shell Air Walker
Database Sync Date
2026-08-09 16:45:40

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 Actimove® Closed Shell Air Walker?

The registered manufacturer of record for Actimove® Closed Shell Air Walker is Span Link International, LLC.

What is the Primary UDI-DI identifier for Actimove® Closed Shell Air Walker?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 01230000153218.

What classification code is assigned to this device?

This device is registered under product classification code Y06120601.

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