USA Universal Cataract Inst Set

GUDID 05060745555857

BLINK MEDICAL LIMITED

Ophthalmic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 05060745555857
• NIH Device Record Key: c2d18693-b3c4-4a95-8890-ff980e77e677
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: USA Universal Cataract Inst Set
• Version Model Number: 76-0026A
• 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	05060745555840 [Primary]
GS1	05060745555857 [Package]; Contains: 05060745555840; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• PZG: Surgical Eye Tray

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: 2022-08-09
• Device Publish Date: 2022-08-01

On-Brand Devices [USA Universal Cataract Inst Set]

• 05060745550715: 76-0026
• 05060745555857: 76-0026A