Ahmed™ Glaucoma Valve S2

GUDID 00892064002133

Polypropylene Glaucoma Drainage Device

NEW WORLD MEDICAL, INCORPORATED

Eye valve

• Primary Device ID: 00892064002133
• NIH Device Record Key: 86ac5462-cff0-45be-a2b7-0d1d4153daac
• Commercial Distribution Discontinuation: 2019-03-01
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Ahmed™ Glaucoma Valve
• Version Model Number: S2
• Catalog Number: S2
• Company DUNS: 622768711
• Company Name: NEW WORLD MEDICAL, INCORPORATED
• Device Count: 1
• DM Exempt: true
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(909)466-4304
• Email: info@ahmedvalve.com

Device Dimensions

• Area/Surface Area: 184 Square millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00892064002133 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K925636

FDA Product Code

• KYF: IMPLANT, EYE VALVE

Sterilization

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

[00892064002133]

Radiation Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-10-22
• Device Publish Date: 2015-03-24

On-Brand Devices [Ahmed™ Glaucoma Valve]

• 00892064002133: Polypropylene Glaucoma Drainage Device
• 00892064002188: Ahmed Accessory Tube Extender
• 00892064002119: Silicone Glaucoma Drainage Device
• 00892064002126: Pediatric Silicone Glaucoma Drainage Device