CyPass

GUDID 10380657540034

CyPass System

Alcon Laboratories, Inc.

Glaucoma shunt

• Primary Device ID: 10380657540034
• NIH Device Record Key: b0936350-2dad-436f-adcc-84ef06d2fc78
• Commercial Distribution Discontinuation: 2018-08-28
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: CyPass
• Version Model Number: 8065754003
• Company DUNS: 008018525
• Company Name: Alcon Laboratories, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)-862-5266
• Email: web.masterus@alcon.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00380657540037 [Primary]
GS1	10380657540034 [Package]; Contains: 00380657540037; Package: BOX [5 Units]; Discontinued: 2018-08-28; Not in Commercial Distribution

FDA Product Code

• OGO: Intraocular Pressure Lowering Implant

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-10-15
• Device Publish Date: 2016-09-16

On-Brand Devices [CyPass]

• 00380657540075: CYPASS ULTRA SYSTEM CYPASS MICRO-STENT CYPASS' APPLIER
• 10380657540034: CyPass System