| Primary Device ID | 30840143903742 |
| NIH Device Record Key | 317871a4-775d-4781-9546-0d9ff00396c2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Lariat RS |
| Version Model Number | 30-06 |
| Catalog Number | FG-0028-02 |
| Company DUNS | 006133784 |
| Company Name | ATRICURE, 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 | 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 | true |
| OTC Over-The-Counter | false |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10840143901713 [Previous] |
| GS1 | 10840143904424 [Primary] |
| GS1 | 30840143903742 [Package] Contains: 10840143904424 Package: Box [1 Units] In Commercial Distribution |
| GS1 | 50840143903272 [Package] Package: Case [10 Units] In Commercial Distribution |
| GAT | Suture, Nonabsorbable, Synthetic, Polyethylene |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-08-06 |
| Device Publish Date | 2021-07-29 |
| 30840143901724 | Suture Delivery Device |
| 30840143903742 | Suture Delivery Device |
| 30840143909447 | LARIAT RS Suture Delivery Device, 45mm |