Dual Bore Cannula 7530

GUDID 10813465011811

Simultaneous infusion of liquid through center lumen and aspiration of fluid through vent hole in outer lumen. Tip Length 4mm

HURRICANE MEDICAL INC

Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

• Primary Device ID: 10813465011811
• NIH Device Record Key: 540f3102-ee22-47b4-9f02-3942b1543ac3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dual Bore Cannula
• Version Model Number: 7530
• Catalog Number: 7530
• Company DUNS: 093377724
• Company Name: HURRICANE MEDICAL INC
• Device Count: 5
• DM Exempt: true
• 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: true
• OTC Over-The-Counter: false

Device Dimensions

• Length: 32 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813465011814 [Primary]
GS1	10813465011811 [Unit of Use]

FDA Product Code

• HMX: Cannula, Ophthalmic

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: true

[10813465011811]

Radiation Sterilization;Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-05-07
• Device Publish Date: 2020-04-29

On-Brand Devices [Dual Bore Cannula]

• 10813465011811: Simultaneous infusion of liquid through center lumen and aspiration of fluid through vent hole i
• 10813465011804: Simultaneous infusion of liquid through center lumen and aspiration of fluid through vent hole i
• 10813465011798: Simultaneous infusion of liquid through center lumen and aspiration of fluid through vent hole i