Boston XO Boston XO

GUDID 00785811435660

Rigid Gas Permeable Contact Lens

BAUSCH & LOMB INCORPORATED

Rigid-gas-permeable corrective contact lens, daily-wear

• Primary Device ID: 00785811435660
• NIH Device Record Key: b7e4233b-92d6-4608-8548-d5765ba70e4e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Boston XO
• Version Model Number: hexafocon A
• Catalog Number: Boston XO
• Company DUNS: 058816302
• 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: false
• 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	00785811435660 [Primary]

FDA Product Code

• HQD: Lens, Contact (Other Material) - Daily

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-10-18

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• 00757770668083 - Bausch + Lomb: 2025-09-22 E0982 RETRACTOR-WORK END COATD
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