BLIS-X0

GUDID 00757770523337

BLIS IOL Delivery System – X0 Cartridge

Bausch & Lomb Incorporated

Posterior-chamber intraocular lens, pseudophakic

• Primary Device ID: 00757770523337
• NIH Device Record Key: dcedd958-18d7-42fa-b410-c28417153340
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BLIS-X0
• Version Model Number: BLIS-X0
• 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: true
• 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	00757770523337 [Primary]

FDA Product Code

• MSS: Folders And Injectors, Intraocular Lens (Iol)

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: 2024-03-12
• Device Publish Date: 2024-03-04

Devices Manufactured by Bausch & Lomb Incorporated

• 00757770425044 - Bausch + Lomb: 2026-02-12 N3520 SUCTION ELEVATOR (DISC)
• 00757770429301 - Bausch + Lomb: 2026-02-12 DUCKBILL ELEVATOR DOUBLE ENDED
• 00757770636631 - Bausch + Lomb: 2026-02-12 E4937 M MANIPULATOR TITANIUM
• 00757770668427 - Bausch + Lomb: 2026-02-12 E5030 ORBITAL RETRACTOR - DISC
• 00757770683741 - Bausch + Lomb: 2026-02-12 E4065 A LIEBERMAN SPEC "V"BLDS
• 00757770708260 - Bausch + Lomb: 2026-02-12 E0983 RETRACTOR-WORK END COATED
• 00757770635382 - Bausch + Lomb: 2026-02-04 TRU-SIZE DIAMOND KNIFE
• 00310119041024 - Bausch + Lomb: 2026-01-19 Soft Contact Lens Disinfecting Solution, Two 12 FL OZ Bottles, 1 Lens Case