renu fresh multi-purpose solution 623122

GUDID 00310119031223

Soft Contact Lens Disinfecting Solution, 4 FL OZ

Bausch & Lomb Incorporated

Multi-purpose soft contact lens solution

• Primary Device ID: 00310119031223
• NIH Device Record Key: d0c18dec-c901-4ce4-a1ea-e4ab93285dba
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: renu fresh multi-purpose solution
• Version Model Number: FCP-4122
• Catalog Number: 623122
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00310119031223 [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: 2025-02-27
• Device Publish Date: 2025-02-19

On-Brand Devices [renu fresh multi-purpose solution]

• 00310119032220: Soft Contact Lens Disinfecting Solution, 2 FL OZ
• 00310119031223: Soft Contact Lens Disinfecting Solution, 4 FL OZ
• 00310119031186: Soft Contact Lens Disinfecting Solution, 4 FL OZ