gudid
Primary ID: 600
Deep Well Lens Case (Ribbed) (UDI 600)
Manufactured by Paragon Vision Sciences, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Deep Well Lens Case (Ribbed) - Primary ID 600
Device Regulatory Overview
The Deep Well Lens Case (Ribbed) (Model/Catalog Number: 600) is a medical device manufactured by Paragon Vision Sciences, Inc.. This product is indexed under FDA Product Code / Category Classification LRX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 600
- Product Code / EMDN
- LRX
- Device Name
- Deep Well Lens Cases are fabricated from a low-density polyethylene plastic resin and have a ribbed lens well surface. They are used for the storage and chemical disinfection of hard, GP or soft contact lenses. They are not to be used with heat disinfection.
- Database Sync Date
- 2026-08-09 09:43:50
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 Deep Well Lens Case (Ribbed)?
The registered manufacturer of record for Deep Well Lens Case (Ribbed) is Paragon Vision Sciences, Inc..
What is the Primary UDI-DI identifier for Deep Well Lens Case (Ribbed)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 600.
What classification code is assigned to this device?
This device is registered under product classification code LRX.
Similar Classification Devices (LRX)
Other Devices by Paragon Vision Sciences, Inc.
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