gudid Primary ID: F9024SSCNE

NA (UDI F9024SSCNE)

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: F9024SSCNE) 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: F9024SSCNE
Product Code / EMDN: DRX
Device Name: Reusable peripheral clamp electrodes for ECG, 30x130mm clamp dimensions. F9024SSCNE has features that make it absolutely reliable during signal recording with all different ECG devices on the market. The electrode metallic part is made of silver coated material, allowing a safe and clear signal transmission. FIAB peripheral electrodes, thanks to screw and clip connections, can be connected to all ECG devices and monitors with patient cable which have plug or snap connections. Black plastic clamp model. The product is latex-free and without Nickel.
Database Sync Date: 2026-08-09 09:05:05

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 F9024SSCNE.

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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