SoFlex® SE IOL LI61SE2200

GUDID 10757770229908

SoFlex SE Silicone Foldable Intraocular Lens +22.00D

Bausch & Lomb Incorporated

Posterior-chamber intraocular lens, pseudophakic

• Primary Device ID: 10757770229908
• NIH Device Record Key: 6ce5a919-8699-4c6c-a8db-deabdfd41576
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SoFlex® SE IOL
• Version Model Number: LI61SE
• Catalog Number: LI61SE2200
• 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: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10757770229908 [Primary]

FDA Product Code

• HQL: intraocular lens

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: 2024-05-29
• Device Publish Date: 2024-05-21

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