Comfortear Lacrisolve 180 Absorbable Punctum Plug

GUDID 00810020082883

Canalicular Plug

RIVERPOINT MEDICAL, LLC

Lacrimal punctum plug

• Primary Device ID: 00810020082883
• NIH Device Record Key: 31bf9b8a-5bb4-40f2-9a8d-f8c496bd9f55
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Comfortear Lacrisolve 180 Absorbable Punctum Plug
• Version Model Number: 42702-174-03
• 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	00810020082883 [Primary]

FDA Product Code

• LZU: Plug, Punctum

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-02-24
• Device Publish Date: 2020-02-14

On-Brand Devices [Comfortear Lacrisolve 180 Absorbable Punctum Plug]

• 00810020082906: Canalicular Plug
• 00810020082890: Canalicular Plug
• 00810020082883: Canalicular Plug
• 00810020082876: Canalicular Plug
• 20810020080821: Canalicular Plug
• 20810020080814: Canalicular Plug
• 20810020080807: Canalicular plug
• 20810020080791: Canalicular plug