Lacrimal Plug

GUDID 00812444028782

Canalicular Plug

RIVERPOINT MEDICAL, LLC

Lacrimal punctum plug Lacrimal punctum plug

• Primary Device ID: 00812444028782
• NIH Device Record Key: 467f9bdd-4704-46f6-a0d9-ba647e940f13
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lacrimal Plug
• Version Model Number: ESK-1005
• Company DUNS: 964053560
• Company Name: RIVERPOINT MEDICAL, LLC
• Device Count: 1
• DM Exempt: false
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812444028782 [Primary]
GS1	10812444028789 [Package]; Package: [10 Units]; In Commercial Distribution

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: 2019-04-12
• Device Publish Date: 2018-10-01

On-Brand Devices [Lacrimal Plug]

• 00812444028782: Canalicular Plug
• 00812444028775: Canalicular Plug
• 00812444028768: Canalicular Plug
• 00812444028744: Canalicular Plug