eudamed_udi
Primary ID: 08057509260734
Reformer (UDI 08057509260734)
Manufactured by IDS S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Reformer - Primary ID 08057509260734
Device Regulatory Overview
The Reformer (Model/Catalog Number: ID-GXCO727) 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-GXCO727
- Product Code / EMDN
- Y0599
- Device Name
- Dispositivo per allenamento cardiovascolare
- Database Sync Date
- 2026-08-09 16:29:05
Full Regulatory Attributes
π Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)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 08057509260734.
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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