gudid
Primary ID: FLX300UV
FLUOREX300UV (UDI FLX300UV)
Manufactured by G. T. LABORATORIES, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FLUOREX300UV - Primary ID FLX300UV
Device Regulatory Overview
The FLUOREX300UV (Model/Catalog Number: FLX300UV) is a medical device manufactured by G. T. LABORATORIES, INC.. This product is indexed under FDA Product Code / Category Classification HQD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FLX300UV
- Product Code / EMDN
- HQD
- Device Name
- Ridgid-gas-permeable corrective contact lens, daily ware
- Database Sync Date
- 2026-08-09 09:43:48
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 FLUOREX300UV?
The registered manufacturer of record for FLUOREX300UV is G. T. LABORATORIES, INC..
What is the Primary UDI-DI identifier for FLUOREX300UV?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FLX300UV.
What classification code is assigned to this device?
This device is registered under product classification code HQD.
Similar Classification Devices (HQD)
Other Devices by G. T. LABORATORIES, INC.
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