gudid Primary ID: F9079P/100

NA (UDI F9079P/100)

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: F9079P/100) is a medical device manufactured by FIAB SPA. This product is indexed under FDA Product Code / Category Classification DRX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: F9079P/100
Product Code / EMDN: DRX
Device Name: Disposable ECG electrodes with solid gel and SSC sensor, oval-shaped 32x36mm and and stainless steel snap. F9079P/100 model is suitable both for rest and stress or Holter ECG recording, with a direct application onto the skin. The SSC sensor permits a reliable and stable recording. The external layer in waterproof medical grade PE foam protects the skin beneath the electrode from air and contaminating fluids.
Database Sync Date: 2026-08-09 09:04:31

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 F9079P/100.

What classification code is assigned to this device?

This device is registered under product classification code DRX.

Similar Classification Devices (DRX)

Other Devices by FIAB SPA

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