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 Issuing Agency | Device ID |
---|---|
GS1 | 00369918645018 [Primary] |
GS1 | 00369918645100 [Direct Marking] |
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
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-23 |
Device Publish Date | 2024-04-15 |
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 |