GUDIDData
eudamed_udi Primary ID: D-FL2827OM4

ONCOFUX (UDI D-FL2827OM4)

Manufactured by Know Medical Srl

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ONCOFUX - Primary ID D-FL2827OM4

Device Regulatory Overview

The ONCOFUX (Model/Catalog Number: FL2 827 O) is a medical device manufactured by Know Medical Srl. This product is indexed under FDA Product Code / Category Classification A03010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
FL2 827 O
Product Code / EMDN
A03010102
Device Name
ONCOFUX - Deflussore chemioterapico 4 vie in PP ambrato con rubinetto
Database Sync Date
2026-08-09 17:03:34

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 ONCOFUX?

The registered manufacturer of record for ONCOFUX is Know Medical Srl.

What is the Primary UDI-DI identifier for ONCOFUX?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-FL2827OM4.

What classification code is assigned to this device?

This device is registered under product classification code A03010102.

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