gudid
Primary ID: VERO Sensor 60
NIOX (UDI VERO Sensor 60)
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 Sensor 60
Device Regulatory Overview
The NIOX (Model/Catalog Number: VERO Sensor 60) 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 Sensor 60
- Product Code / EMDN
- MXA
- Device Name
- The NO sensor for NIOX VERO utilizes analytical electrochemical sensor technology. The NO sensor is pre-programmable for a defined number of tests: 60100300500 or 1000 tests.
- 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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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 Sensor 60.
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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