SUPEREAGLE

GUDID 00844505010542

SUPEREAGLE PUNCTUM PLUG LARGE SILICONE TWIN PACK

EAGLE VISION, INC.

Lacrimal punctum plug

• Primary Device ID: 00844505010542
• NIH Device Record Key: 5b77ec24-876b-44d9-85db-af49258d3509
• Commercial Distribution Discontinuation: 2017-03-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: SUPEREAGLE
• Version Model Number: 31322
• Company DUNS: 174318360
• Company Name: EAGLE VISION, INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• 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

Customer Support Contacts

• Phone: 1-800-222-7584
• Email: info@eaglevis.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00844505010542 [Primary]

FDA Product Code

• LZU: Plug, Punctum

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-26

On-Brand Devices [SUPEREAGLE]

• 00844505010559: SUPEREAGLE PUNCTUM PLUG MEDIUM SILICONE TWIN PACK
• 00844505010542: SUPEREAGLE PUNCTUM PLUG LARGE SILICONE TWIN PACK
• 00844505010535: SUPEREAGLE PUNCTUM PLUG SMALL SILICONE TWIN PACK