Lester IOL Manipulator

GUDID 05060745557691

BLINK MEDICAL LIMITED

Ophthalmic surgical probe, single-use

• Primary Device ID: 05060745557691
• NIH Device Record Key: ea997fc8-b4e3-4de2-b3d1-11987a7d9375
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lester IOL Manipulator
• Version Model Number: 41-1007
• Company DUNS: 738288096
• Company Name: BLINK MEDICAL LIMITED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060745557684 [Primary]
GS1	05060745557691 [Package]; Contains: 05060745557684; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• HND: Spatula, Ophthalmic
• HNQ: Hook, Ophthalmic

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: 2023-12-05
• Device Publish Date: 2023-11-27

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• 05060480402256 - Manipulator Spatula Govan: 2024-05-29