Bausch & Lomb FCP-4360

GUDID 00310119041086

Soft Contact Lens Disinfecting Solution, Two 16 Bottles, 1 Lens Case

Bausch & Lomb Incorporated

Contact lens care kit

• Primary Device ID: 00310119041086
• NIH Device Record Key: f46f5694-2ad2-4ea9-843d-c7d87b841dde
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bausch & Lomb
• Version Model Number: 624423
• Catalog Number: FCP-4360
• Company DUNS: 196603781
• Company Name: Bausch & Lomb Incorporated
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00310119041086 [Primary]

FDA Product Code

• LPN: Accessories, Soft Lens Products

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-01-19
• Device Publish Date: 2026-01-09

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• 00310119041086: Soft Contact Lens Disinfecting Solution, Two 16 Bottles, 1 Lens Case