gudid
Primary ID: 7469
Bausch + Lomb (UDI 7469)
Manufactured by Bausch & Lomb Incorporated
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bausch + Lomb - Primary ID 7469
Device Regulatory Overview
The Bausch + Lomb (Model/Catalog Number: 7469) is a medical device manufactured by Bausch & Lomb Incorporated. This product is indexed under FDA Product Code / Category Classification MRC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7469
- Product Code / EMDN
- MRC
- Device Name
- One 1 FL OZ Conditioning, One 0.33 FL OZ Cleaner, 1 Lens Case
- Database Sync Date
- 2026-08-09 09:08:50
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 Bausch + Lomb?
The registered manufacturer of record for Bausch + Lomb is Bausch & Lomb Incorporated.
What is the Primary UDI-DI identifier for Bausch + Lomb?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7469.
What classification code is assigned to this device?
This device is registered under product classification code MRC.
Similar Classification Devices (MRC)
Other Devices by Bausch & Lomb Incorporated
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