Primary Device ID | 10840277405101 |
NIH Device Record Key | 9709f467-6481-411c-a409-f963aed11152 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lacrimal Plug |
Version Model Number | 58142 |
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 | true |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00840277405104 [Primary] |
GS1 | 10840277405101 [Package] Contains: 00840277405104 Package: [10 Units] In Commercial Distribution |
LZU | Plug, Punctum |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-10-24 |
Device Publish Date | 2024-10-16 |
00812444028782 | Canalicular Plug |
00812444028775 | Canalicular Plug |
00812444028768 | Canalicular Plug |
00812444028744 | Canalicular Plug |
10840277405125 | CANALICULAR PLUG |
10840277405118 | CANALICULAR PLUG |
10840277405101 | CANALICULAR PLUG |
10840277405095 | CANALICULAR PLUG |