Sub-Tenon's Cannula 1327

GUDID 00813465010107

For administering local anesthetic agents prior to ophthalmic surgery.

HURRICANE MEDICAL INC

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

• Primary Device ID: 00813465010107
• NIH Device Record Key: a8a3be3a-7183-4c40-b709-9a377bf81f9e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sub-Tenon's Cannula
• Version Model Number: 1327
• Catalog Number: 1327
• 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

• Length: 22 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813465010107 [Primary]
GS1	10813465010104 [Unit of Use]

FDA Product Code

• HMX: Cannula, Ophthalmic

Sterilization

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

[00813465010107]

Radiation Sterilization;Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-04-07
• Device Publish Date: 2020-01-21