Comfortear Lacrisolve 180 Absorbable Punctum Plug

GUDID 20810020080814

Canalicular Plug

RIVERPOINT MEDICAL, LLC

Lacrimal punctum plug

• Primary Device ID: 20810020080814
• NIH Device Record Key: 1b7d18f5-7ebb-4c24-969b-54c8834c39d7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Comfortear Lacrisolve 180 Absorbable Punctum Plug
• Version Model Number: 42702-177-04
• 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	00810020080810 [Primary]
GS1	20810020080814 [Package]; Contains: 00810020080810; 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: 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