gudid Primary ID: F9007PL

NA (UDI F9007PL)

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: F9007PL) 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: F9007PL
Product Code / EMDN: DRX
Device Name: Rubber balls for FIAB suction chest electrodes, 25mm dimensions. F9007PL model is used as a replacement of old rubber balls. They are made of blue PVC-light version. LATEX free.
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 F9007PL.

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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