FLUOREX(TM) RIGID GAS PERMEABLE CONTACT LENS (UDI P880001)
Manufactured by G.T. Laboratories, Inc.
Device Regulatory Overview
The FLUOREX(TM) RIGID GAS PERMEABLE CONTACT LENS (Model/Catalog Number: Unspecified) 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
- N/A
- Product Code / EMDN
- HQD
- Device Name
- Lens, contact (other material) - daily
- Database Sync Date
- 2026-08-09 10:04:44
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 FLUOREX(TM) RIGID GAS PERMEABLE CONTACT LENS?
The registered manufacturer of record for FLUOREX(TM) RIGID GAS PERMEABLE CONTACT LENS is G.T. Laboratories, Inc..
What is the Primary UDI-DI identifier for FLUOREX(TM) RIGID GAS PERMEABLE CONTACT LENS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P880001.
What classification code is assigned to this device?
This device is registered under product classification code HQD.
Similar Classification Devices (HQD)
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