gudid Primary ID: Apps / Panel

NIOX (UDI Apps / Panel)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NIOX (Model/Catalog Number: Apps / Panel) is a medical device manufactured by Circassia AB. This product is indexed under FDA Product Code / Category Classification MXA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Apps / Panel
Product Code / EMDN: MXA
Device Name: NIOX Apps / Panel is an optional software accessory allowing an additional display for the NIOX serise of Airway Inflammation Monitors including the NIOX MINO 09 and NIOX VERO devices.
Database Sync Date: 2026-08-09 09:48:57

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 NIOX?

The registered manufacturer of record for NIOX is Circassia AB.

What is the Primary UDI-DI identifier for NIOX?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Apps / Panel.

What classification code is assigned to this device?

This device is registered under product classification code MXA.

Similar Classification Devices (MXA)

Other Devices by Circassia AB

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