GUDIDData
eudamed_udi Primary ID: 04057027830444

motionLine-E (UDI 04057027830444)

Manufactured by UFSK-International OSYS GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for motionLine-E - Primary ID 04057027830444

Device Regulatory Overview

The motionLine-E (Model/Catalog Number: 17000001) is a medical device manufactured by UFSK-International OSYS GmbH. This product is indexed under FDA Product Code / Category Classification V080502 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
17000001
Product Code / EMDN
V080502
Device Name
Transport- and relaxing chair
Database Sync Date
2026-08-09 16:47:23

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 motionLine-E?

The registered manufacturer of record for motionLine-E is UFSK-International OSYS GmbH.

What is the Primary UDI-DI identifier for motionLine-E?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04057027830444.

What classification code is assigned to this device?

This device is registered under product classification code V080502.

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