Side Cutting Cystotome 3725

GUDID 00813465010596

Creates opening into anterior capsule during cataract treatment.

HURRICANE MEDICAL INC

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

• Primary Device ID: 00813465010596
• NIH Device Record Key: bc440ad5-5016-4f6e-860e-5f74fa9335a4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Side Cutting Cystotome
• Version Model Number: 3725
• Catalog Number: 3725
• Company DUNS: 093377724
• Company Name: HURRICANE MEDICAL INC
• Device Count: 1
• 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: 16 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813465010596 [Primary]
GS1	10813465010593 [Unit of Use]

FDA Product Code

• HNY: Cystotome

Sterilization

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

[00813465010596]

Ethylene Oxide;Radiation Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-02-17
• Device Publish Date: 2020-01-22

On-Brand Devices [Side Cutting Cystotome]

• 08134650137259: Creates opening into anterior capsule during cataract treatment.
• 00813465010596: Creates opening into anterior capsule during cataract treatment.