Lasik Cannula - Daya 7121

GUDID 10813465011224

For LASIK surgery and other types of refractive surgery.

HURRICANE MEDICAL INC

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

• Primary Device ID: 10813465011224
• NIH Device Record Key: 3a661575-7ca3-4484-af58-102c7ac054c9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lasik Cannula - Daya
• Version Model Number: 7121
• Catalog Number: 7121
• Company DUNS: 093377724
• Company Name: HURRICANE MEDICAL INC
• Device Count: 10
• 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

• Needle Gauge: 21 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813465011227 [Primary]
GS1	10813465011224 [Unit of Use]

FDA Product Code

• HMX: Cannula, Ophthalmic

Sterilization

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

[10813465011224]

Radiation Sterilization;Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-04-21
• Device Publish Date: 2020-04-13

On-Brand Devices [Lasik Cannula - Daya]

• 10813465011231: For LASIK surgery and other types of refractive surgery.
• 10813465011224: For LASIK surgery and other types of refractive surgery.