Sub-Tenon's Cannula 1320

GUDID 00813465010091

Used for administering local anesthetic prior to ophthalmic surgery.

HURRICANE MEDICAL INC

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

• Primary Device ID: 00813465010091
• NIH Device Record Key: c3fdb427-33f0-42f3-9f91-4a0655c64755
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sub-Tenon's Cannula
• Version Model Number: 1320
• Catalog Number: 1320
• 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: 20 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813465010091 [Primary]
GS1	10813465010098 [Unit of Use]

FDA Product Code

• HMX: Cannula, Ophthalmic

Sterilization

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

[00813465010091]

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