eudamed_udi Primary ID: 08057509262585

Reformer (UDI 08057509262585)

Manufactured by IDS S.r.l.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Reformer (Model/Catalog Number: ID-CY-S2001) is a medical device manufactured by IDS S.r.l.. This product is indexed under FDA Product Code / Category Classification Y0599 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ID-CY-S2001
Product Code / EMDN: Y0599
Device Name: Dispositivo per allenamento cardiovascolare
Database Sync Date: 2026-08-09 17:49:21

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 Reformer?

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

What is the Primary UDI-DI identifier for Reformer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057509262585.

What classification code is assigned to this device?

This device is registered under product classification code Y0599.

Similar Classification Devices (Y0599)

Other Devices by IDS S.r.l.

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