Lacrifill Canalicular Gel

GUDID 00369918645100

Canalicular gel

AMRING PHARMACEUTICALS INC.

Scalpel, single-use Scalpel, single-use Scalpel, single-use Scalpel, single-use Scalpel, single-use Scalpel, single-use Scalpel, single-use Scalpel, single-use Scalpel, single-use Scalpel, single-use Scalpel, single-use Scalpel, single-use Scalpel, single-use Scalpel, single-use Scalpel, single-use Scalpel, single-use Scalpel, single-use

• Primary Device ID: 00369918645100
• NIH Device Record Key: b39354a9-f08b-49c9-8ce5-ecc421de1dad
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lacrifill Canalicular Gel
• Version Model Number: V1
• Company DUNS: 079843051
• Company Name: AMRING PHARMACEUTICALS INC.
• 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00369918645018 [Primary]
GS1	00369918645100 [Direct Marking]

Sterilization

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

[00369918645100]

Dry Heat Sterilization

[00369918645100]

Dry Heat Sterilization

[00369918645100]

Dry Heat Sterilization

[00369918645100]

Dry Heat Sterilization

[00369918645100]

Dry Heat Sterilization

[00369918645100]

Dry Heat Sterilization

[00369918645100]

Dry Heat Sterilization

[00369918645100]

Dry Heat Sterilization

[00369918645100]

Dry Heat Sterilization

[00369918645100]

Dry Heat Sterilization

[00369918645100]

Dry Heat Sterilization

[00369918645100]

Dry Heat Sterilization

[00369918645100]

Dry Heat Sterilization

[00369918645100]

Dry Heat Sterilization

[00369918645100]

Dry Heat Sterilization

[00369918645100]

Dry Heat Sterilization

[00369918645100]

Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-23
• Device Publish Date: 2024-04-15

Devices Manufactured by AMRING PHARMACEUTICALS INC.

• 00369918645100 - Lacrifill Canalicular Gel: 2024-04-23Canalicular gel
• 00369918645100 - Lacrifill Canalicular Gel: 2024-04-23 Canalicular gel
• 01369918000007 - Biolon: 2018-07-06 Viscoelastic surgical aid