gudid
Primary ID: 034
FLOSI (UDI 034)
Manufactured by LAGADO CORPORATION, THE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FLOSI - Primary ID 034
Device Regulatory Overview
The FLOSI (Model/Catalog Number: 034) is a medical device manufactured by LAGADO CORPORATION, THE. This product is indexed under FDA Product Code / Category Classification HQD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 034
- Product Code / EMDN
- HQD
- Device Name
- FLOSI Fuoro-silicone Acrylat daily wear contact lens
- Database Sync Date
- 2026-08-09 09:49:26
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 FLOSI?
The registered manufacturer of record for FLOSI is LAGADO CORPORATION, THE.
What is the Primary UDI-DI identifier for FLOSI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 034.
What classification code is assigned to this device?
This device is registered under product classification code HQD.
Similar Classification Devices (HQD)
Other Devices by LAGADO CORPORATION, THE
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