eudamed_udi
Primary ID: 08052990117406
FPO 100 (UDI 08052990117406)
Manufactured by F.G.P. s.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FPO 100 - Primary ID 08052990117406
Device Regulatory Overview
The FPO 100 (Model/Catalog Number: FPO-100.M.30) is a medical device manufactured by F.G.P. s.r.l.. This product is indexed under FDA Product Code / Category Classification Y060499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FPO-100.M.30
- Product Code / EMDN
- Y060499
- Device Name
- ORTESI ADDOMINALI - ALTRE - FASCE ADDOMINALI
- Database Sync Date
- 2026-08-09 16:29:33
Full Regulatory Attributes
đź”’ Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of FPO 100?
The registered manufacturer of record for FPO 100 is F.G.P. s.r.l..
What is the Primary UDI-DI identifier for FPO 100?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052990117406.
What classification code is assigned to this device?
This device is registered under product classification code Y060499.
Similar Classification Devices (Y060499)
Other Devices by F.G.P. s.r.l.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint