gudid
Primary ID: VX40 APS
Visionix (UDI VX40 APS)
Manufactured by LUNEAU TECHNOLOGY OPERATIONS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Visionix - Primary ID VX40 APS
Device Regulatory Overview
The Visionix (Model/Catalog Number: VX40 APS) is a medical device manufactured by LUNEAU TECHNOLOGY OPERATIONS. This product is indexed under FDA Product Code / Category Classification HLM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VX40 APS
- Product Code / EMDN
- HLM
- Device Name
- Database Sync Date
- 2026-08-09 09:52:17
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 Visionix?
The registered manufacturer of record for Visionix is LUNEAU TECHNOLOGY OPERATIONS.
What is the Primary UDI-DI identifier for Visionix?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VX40 APS.
What classification code is assigned to this device?
This device is registered under product classification code HLM.
Similar Classification Devices (HLM)
Other Devices by LUNEAU TECHNOLOGY OPERATIONS
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