NA (UDI F6749RUSA)

Manufactured by FIAB SPA

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NA (Model/Catalog Number: F6749RUSA) is a medical device manufactured by FIAB SPA. This product is indexed under FDA Product Code / Category Classification IKD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: F6749RUSA
Product Code / EMDN: IKD
Device Name: ECG patient cables 10 leads with defibrillator protection, Resistance 10 kOhm, with 4mm plug.
Database Sync Date: 2026-08-09 09:04:39

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 NA?

The registered manufacturer of record for NA is FIAB SPA.

What is the Primary UDI-DI identifier for NA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is F6749RUSA.

What classification code is assigned to this device?

This device is registered under product classification code IKD.

Similar Classification Devices (IKD)

Other Devices by FIAB SPA

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