gudid
Primary ID: VERO
NIOX (UDI VERO)
Manufactured by Circassia AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NIOX - Primary ID VERO
Device Regulatory Overview
The NIOX (Model/Catalog Number: VERO) 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
- Product Code / EMDN
- MXA
- Device Name
- NIOX VERO measures Nitric Oxide (NO) in human breath. Nitric Oxide is frequently increased in some inflammatory processes such as asthma. The fractional NO concentration in expired breath (FeNO), can be measured by NIOX VERO according to guidelines for NO measurement established by the American Thoracic Society.
- Database Sync Date
- 2026-08-09 09:48:57
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)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.
What classification code is assigned to this device?
This device is registered under product classification code MXA.
Similar Classification Devices (MXA)
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