Sub Tenon Set - Fine Tip

GUDID 05060745558094

BLINK MEDICAL LIMITED

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

• Primary Device ID: 05060745558094
• NIH Device Record Key: ce3ba5fc-86da-4966-bb61-a67c7c1a71ce
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sub Tenon Set - Fine Tip
• Version Model Number: 002
• 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	05060745558087 [Primary]
GS1	05060745558094 [Package]; Contains: 05060745558087; Package: [8 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: 2024-05-29
• Device Publish Date: 2024-05-21

On-Brand Devices [Sub Tenon Set - Fine Tip]

• 05060480403031: 001-A
• 05060745558094: 002