gudid
Primary ID: 0222
VixOne (UDI 0222)
Manufactured by SUNMED, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VixOne - Primary ID 0222
Device Regulatory Overview
The VixOne (Model/Catalog Number: 0222) is a medical device manufactured by SUNMED, LLC. This product is indexed under FDA Product Code / Category Classification CAF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0222
- Product Code / EMDN
- CAF
- Device Name
- VixOne Small Volume Nebulizer
- Database Sync Date
- 2026-08-09 09:04:13
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 VixOne?
The registered manufacturer of record for VixOne is SUNMED, LLC.
What is the Primary UDI-DI identifier for VixOne?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0222.
What classification code is assigned to this device?
This device is registered under product classification code CAF.
Similar Classification Devices (CAF)
Other Devices by SUNMED, LLC
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