gudid Primary ID: VERO Battery

NIOX (UDI VERO Battery)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NIOX (Model/Catalog Number: VERO Battery) 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: VERO Battery
Product Code / EMDN: MXA
Device Name: This is a rechargeable Li-Ion replacement battery for the NIOX VERO that is charged via the power supply or USB port.
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 VERO Battery.

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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