GUDIDData
eudamed_udi Primary ID: 08057509260246

Rollator (UDI 08057509260246)

Manufactured by IDS S.r.l.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rollator - Primary ID 08057509260246

Device Regulatory Overview

The Rollator (Model/Catalog Number: ID-RO500) is a medical device manufactured by IDS S.r.l.. This product is indexed under FDA Product Code / Category Classification Y120609 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ID-RO500
Product Code / EMDN
Y120609
Device Name
Rollator
Database Sync Date
2026-08-09 17:06:10

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 Rollator?

The registered manufacturer of record for Rollator is IDS S.r.l..

What is the Primary UDI-DI identifier for Rollator?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057509260246.

What classification code is assigned to this device?

This device is registered under product classification code Y120609.

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