Boston XO2 Boston XO2

GUDID 00785811435677

Rigid Gas Permeable Contact Lens

BAUSCH & LOMB INCORPORATED

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

• Primary Device ID: 00785811435677
• NIH Device Record Key: 30d72a08-8419-4a4c-8f59-092be5042b81
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Boston XO2
• Version Model Number: hexafocon B
• Catalog Number: Boston XO2
• 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	00785811435677 [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: 2017-10-24

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• 00757770411061 - Bausch + Lomb: 2025-04-25 RETRACTOR LID DESMARRES 1
• 00757770411399 - Bausch + Lomb: 2025-04-25 RETRACTOR ORBITAL SCHEPENS
• 00757770411412 - Bausch + Lomb: 2025-04-25 STEP DIA KNIFE TRIFALET
• 00757770414697 - Bausch + Lomb: 2025-04-25 RETRACTOR LID DESMARRES 0