Connor Wand

GUDID 05060745554874

BLINK MEDICAL LIMITED

Ocular hook/spatula/manipulator, single-use

• Primary Device ID: 05060745554874
• NIH Device Record Key: 9c7a0c15-18fd-441e-961f-47438f08d42c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Connor Wand
• Version Model Number: 41-4013
• 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	05060745554874 [Primary]
GS1	05060745554881 [Package]; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• HND: Spatula, 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: 2022-07-08
• Device Publish Date: 2022-06-30

On-Brand Devices [Connor Wand]

• 05060745554874: 41-4013
• 05056785303343: 41-4013BNS