gudid Primary ID: 12-4000-02

Phadia 5000E+E (UDI 12-4000-02)

Manufactured by Phadia AB

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Phadia 5000E+E (Model/Catalog Number: 12-4000-02) is a medical device manufactured by Phadia AB. This product is indexed under FDA Product Code / Category Classification NHX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 12-4000-02
Product Code / EMDN: NHX
Device Name: Phadia 5000E+E
Database Sync Date: 2026-08-09 09:48:59

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 Phadia 5000E+E?

The registered manufacturer of record for Phadia 5000E+E is Phadia AB.

What is the Primary UDI-DI identifier for Phadia 5000E+E?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 12-4000-02.

What classification code is assigned to this device?

This device is registered under product classification code NHX.

Similar Classification Devices (NHX)

Other Devices by Phadia AB

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