Den VA Cataract Instrument Pack

GUDID 05056785301363

BLINK MEDICAL LIMITED

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

• Primary Device ID: 05056785301363
• NIH Device Record Key: a71ba36c-3577-4549-86c1-aab01ff7020a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Den VA Cataract Instrument Pack
• Version Model Number: 67-0021
• 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: true
• 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	05056785301356 [Primary]
GS1	05056785301363 [Package]; Contains: 05056785301356; 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: 2024-12-26
• Device Publish Date: 2024-12-18

Devices Manufactured by BLINK MEDICAL LIMITED

• 05056785301363 - Den VA Cataract Instrument Pack: 2024-12-26
• 05056785301363 - Den VA Cataract Instrument Pack: 2024-12-26
• 05060745559572 - Meibomian Gland Expression Forceps: 2024-10-16
• 05060745558940 - Scissors Suture Removal: 2024-06-20
• 05060480400009 - Forceps Angled Jewellers 4mm Tip: 2024-05-29
• 05060480400139 - Forceps Epilation Angled: 2024-05-29
• 05060480400436 - Scissors Mayo Curved 13.5cm: 2024-05-29
• 05060480407701 - Manipulator Spatula: 2024-05-29
• 05060480402256 - Manipulator Spatula Govan: 2024-05-29