gudid
Primary ID: 09.151
Loox (UDI 09.151)
Manufactured by Camden Passage Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Loox - Primary ID 09.151
Device Regulatory Overview
The Loox (Model/Catalog Number: 09.151) is a medical device manufactured by Camden Passage Inc. This product is indexed under FDA Product Code / Category Classification LPL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 09.151
- Product Code / EMDN
- LPL
- Device Name
- Aqua Cat Contact Lenses
- Database Sync Date
- 2026-08-09 09:04:19
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 Loox?
The registered manufacturer of record for Loox is Camden Passage Inc.
What is the Primary UDI-DI identifier for Loox?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09.151.
What classification code is assigned to this device?
This device is registered under product classification code LPL.
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