gudid
Primary ID: VT54WW6
Verilux (UDI VT54WW6)
Manufactured by BEAR DOWN CONSULTING
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Verilux - Primary ID VT54WW6
Device Regulatory Overview
The Verilux (Model/Catalog Number: VT54WW6) is a medical device manufactured by BEAR DOWN CONSULTING. This product is indexed under FDA Product Code / Category Classification KZF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VT54WW6
- Product Code / EMDN
- KZF
- Device Name
- Database Sync Date
- 2026-08-09 09:12:28
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 Verilux?
The registered manufacturer of record for Verilux is BEAR DOWN CONSULTING.
What is the Primary UDI-DI identifier for Verilux?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VT54WW6.
What classification code is assigned to this device?
This device is registered under product classification code KZF.
Similar Classification Devices (KZF)
Other Devices by BEAR DOWN CONSULTING
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